Established in the year2004, we, “Shreeji Pharma International”, are one of the leading manufacturers, exporters and suppliers of a range ofPharmaceutical Products. The offered range is formulated using superior quality ingredients, which are procured from the most reliable vendors of the market. These products possess features like safe consumption, accurate composition, precise pH value and non-toxic. The entire range is demanded by our clients for curing various diseases, ailments and health problems.
We have established a state-of-the-art, which is spread across a vast stretch of land situated atVadodarain the state ofGujarat,India. This infrastructure is segregated into various units that are equipped with modern machines and latest technology. All the units are manned by a team of professionals, who are well-experienced in their respective domain. These professionals make sure that the entire production process is undertaken following strict quality standards. Our logistics personnel strive hard to deliver the ordered consignments at clients doorsteps within the given period of time. Further, we have been able to gain trade membership withPharmexcil, IDMAthat has enabled us to serve numerous patrons across theSouth/West Africa, East Europe, East Asia, Central Americaand many more.
Product Details:
| Minimum Order Quantity | 25 Kg |
| API Name | Sertaconazole Nitrate |
| Strength | 1% w/w |
| Grade Standard | USP |
| Packaging Size | 30 gm |
| Prescription/Non prescription | Prescription |
| Physical Form | Powder |
| Therapeutic Class | Antacid |
| Purity | >98% |
| Usage/Application | Pharma |
| Form | Powder |
| Packaging Type | lemi tube |
| Composition | SERTACNAZOLE NITRATE 2% |
| Treatment | Mecetronium ethylsulphate; Ortho-phenylphenol; Surgical hand disinfection; Sustained effect. |
| Shelf life | 2 years. |
| Storage Condition | Room Temperature |
| CAS Number | 99592-39-9 |
| Color | white |
| Dosage Form | 16 times the maximum recommended human dose based on a body surface area comparison |
| Solubility | water |
| Molecular Weight | 500.78 |
| Type Of API | SERTACONAZOLE NITRATE API with Drug Master Files (DMF),CEP/COS |
| Type Of Medicines | It is available in topical formulations for the treatment of skin infections such as athlete's foot. |
| Chemical Name | Sertaconazole nitrate 99592-39-9 Dermofix Ertaczo Zalain |
| Chemical Formula | C20H16Cl3N3O4S |
| Iupac Name | 1-[2-[(7-chloro-1-benzothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazole;nitric acid |
| Molecular Formula | C20H16Cl3N3O4S |
| Brand | Shreeji |
| Flash Point | 325.2degC |
| Formula | C20H15Cl3N2OS.HNO3 |
| Boiling Point | 614.1degC at 760 mmHg |
We are offering high quality of Sertaconazole Nitrate Powder. We are known for manufacturing, exporting, distributing, trading and supplying Sertaconazole Nitrate Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Sertaconazole Nitrate Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Sertaconazole Nitrate Powder. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Sertaconazole Nitrate Powder as well as Intermediates of Sertaconazole Nitrate Powder. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Sertaconazole Nitrate Powder to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Sertaconazole nitrate is a synthetic antifungal agent belonging to the imidazole class, primarily used for topical treatment of fungal infections such as athlete's foot (tinea pedis) and other cutaneous mycoses. Chemical Properties:
Chemical Name: 1-[2-[(7-Chloro-1-benzothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazole nitrate
Molecular Formula: C₂₀H₁₆Cl₃N₃O₄S
Molecular Weight: 500.8 g/mol CAS Number: 99592-32-2
Appearance: White to pale yellow solid Melting Point: 146-147°C
Solubility: Practically insoluble in water (<0.01%); slightly soluble in acetone (0.95%); fairly soluble in ethanol (1.7%) and chloroform (1.5%)
Mechanism of Action:
Sertaconazole nitrate inhibits the synthesis of ergosterol, an essential component of fungal cell membranes, by targeting the cytochrome P-450 sterol C-14 alpha-demethylation process. This disruption leads to increased membrane permeability and leakage of intracellular components, effectively inhibiting fungal growth.
Antimicrobial Activity:
This agent exhibits broad-spectrum antifungal activity against various pathogenic fungi, including dermatophytes and yeasts.
Stability:
Sertaconazole nitrate is extremely stable under various conditions, both in solid form and in suspension. Studies have shown that it remains stable for over five years when stored in tightly sealed amber glass bottles under normal conditions.
Usage:
Sertaconazole nitrate is formulated as a topical cream for the treatment of superficial fungal infections. It is applied directly to the affected area as prescribed by a healthcare provider.
For more detailed information, including potential side effects and contraindications, consult a healthcare professional or refer to official prescribing information.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Molecular Weight | 18.02 g/mol |
| Physical State | Solid |
| Grade Standard | Industrial Grade |
| Purity % | >99% |
| Chemical Formula | C2nH4n+2On+1 |
| EC No. | 500-038-2 |
| Usage/Application | Surfactants, Inactive substance for drugs, Osmotic laxatives |
| Packaging Details | 200 kg Drum |
| Synonyms | PEG, poly(oxyethylene), poly(ethylene oxide) |
| Density | 1.12 g/cm.cu |
| Melting Point | 62.2 DegreeC |
| Boiling Point | 250 DegreeC |
| Viscosity | 90.0 cSt at 25 DegreeC |
We are offering high quality of Polyethylene Glycol PEG. We are known for manufacturing, exporting, distributing, trading and supplying Polyethylene Glycol PEG in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Polyethylene Glycol PEG in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Polyethylene Glycol PEG. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who are manufacturing Polyethylene Glycol PEG as well as Intermediates of Polyethylene Glycol PEG.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Polyethylene Glycol PEG to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
1. Introduction: Polyethylene Glycol (PEG) is a polyether compound derived from ethylene glycol. It is a versatile polymer widely used in pharmaceuticals, cosmetics, food, and industrial applications due to its solubility in water and organic solvents, low toxicity, and non-immunogenic properties.
2. Chemical Structure and Properties: Chemical Formula: H(OCH₂CH₂)ₙOH, Molecular Weight: Varies (from a few hundred to several million Daltons), Appearance: Colorless to slightly yellowish viscous liquid (low MW) or solid (high MW), Solubility: Highly soluble in water, alcohols, acetone, and some organic solvents, Boiling Point: Varies with molecular weight, Melting Point: Also dependent on molecular weight
3. Applications: A. Pharmaceutical & Medical Applications: Excipient in Drug Formulations: Used as a solvent, binder, or carrier in tablets, ointments, and capsules. Laxatives (PEG 3350): Commonly used as an osmotic laxative (e.g., MiraLAX). Eye Drops & Nasal Sprays: Used as a lubricant in ophthalmic solutions. B. Cosmetics & Personal Care Moisturizers & Lotions: Acts as a humectant to retain moisture. Toothpaste & Shampoos: Used for texture and solubility. Lip Balms & Ointments: Helps in even application and smoothness.C. Food Industry: Food Additive (E1521): Used as a carrier, anti-foaming agent, and thickener in food products. Coatings & Packaging: Helps in food processing and packaging Materials.
4. Safety and Toxicity: Low Toxicity: Considered safe for human consumption and medical use.
Biodegradability: PEGs degrade slowly but are considered environmentally safe.
Allergic Reactions: Rare, but some people may experience hypersensitivity.
5. Regulatory Status:PEG is approved by regulatory bodies such as:
FDA (U.S. Food and Drug Administration) – Approved for pharmaceutical and food use.
EMA (European Medicines Agency) – Approved for drug formulations.
EFSA (European Food Safety Authority) – Approved as a food additive (E1521).
6. Conclusion: Polyethylene Glycol (PEG) is a highly versatile compound with applications in pharmaceuticals, cosmetics, food, and industry. Its safety, solubility, and functional properties make it essential in many formulations. However, its usage should be carefully regulated based on molecular weight and application-specific guidelines.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Prescription/Non prescription | Non prescription |
| Packaging Type | Drum |
| Type of API | Digestive System API |
| Packaging Size | 25 |
| Manufacturer | Shreeji |
| Shelf life | 5 Years |
| Country of Origin | Made in India |
| CAS ID | 389-08-2 |
| Elimination Half Life | 6-7 hours,significantly longer in renal impairment |
| Formula | C12H12N2O3 |
| Molar Mass | 232.235g/mol |
| Protein Binding | 90% |
| Metabolism | Metabolized in the liver to active and inactive metabolites. |
| Excretion | Primarily excreted via the kidneys (renal elimination). |
We are offering high quality of Nalidixic Acid . We are known for manufacturing, exporting, distributing, trading and supplying Nalidixic Acid in in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Nalidixic Acid in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Nalidixic Acid . Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Nalidixic Acid as well as Intermediates of Nalidixic Acid .
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Nalidixic Acid to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
General Information
Nalidixic Acid is a synthetic antibacterial agent belonging to the quinolone class. It was the first quinolone antibiotic developed and is primarily effective against Gram-negative bacteria. It is commonly used in veterinary and clinical settings for the treatment of urinary tract infections (UTIs).
Chemical and Physical Properties
Chemical Name: 1-Ethyl-7-methyl-1,8-naphthyridin-4-one-3-carboxylic acid
Molecular Formula: C₁₂H₁₂N₂O₃
Molecular Weight: 232.24 g/mol
CAS Number: 389-08-2
Appearance: White to pale yellow crystalline powder
Solubility: Slightly soluble in water, more soluble in organic solvents (e.g., ethanol, acetone)
Melting Point: 225-230°C
pH: Slightly acidic in aqueous solution
Mode of Action
Nalidixic Acid works by inhibiting DNA gyrase (topoisomerase II), an essential enzyme required for bacterial DNA replication, transcription, and repair. This leads to bacterial cell death, making it a bactericidal agent.
Applications & Uses
Medical Use:Primarily used for urinary tract infections (UTIs) caused by Gram-negative bacteria such as Escherichia coli, Klebsiella spp., Enterobacter spp., and Proteus spp.
Sometimes used in veterinary medicine for bacterial infections in animals.
Rarely used today due to the development of more effective fluoroquinolones.
Research Applications:Used in microbiology and laboratory studies to understand bacterial resistance mechanisms.
Employed in bacterial culture media to select for quinolone-resistant strains.
Industrial & Agricultural Uses:May be used in certain veterinary formulations to control infections in livestock.
Dosage & Administration
Oral Administration (tablet or suspension) is the most common form.
Standard dose for adults: 500-1000 mg every 6 hours for 1-2 weeks (varies by infection severity).
Pediatric use is limited due to possible side effects.
Side Effects & Precautions
Common Side Effects: Nausea, vomiting, diarrhea, Headache, dizziness, Photosensitivity (skin reaction to sunlight)
CNS effects: Seizures, confusion (especially in elderly patients), (though less common than fluoroquinolones)
Contraindications:Not recommended for patients with kidney disease or G6PD deficiency.
Avoid use in children under 12 years and pregnant women.
Should not be taken with antacids or dairy products, as they reduce absorption.
Storage & Stability
Store in a cool, dry place away from light.
Keep at room temperature (15-30°C).
Avoid exposure to moisture and air, as it may degrade.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Prescription/Non prescription | Prescription |
| Type of API | Anti Infective API |
| Brand | shreeji |
| Shelf life | years |
| Melting Point | 189-191degC (lit.) |
| Density | 1.301 g/cm3 |
| Solubility | 15 mg/mL in water |
| Molecular Weight | 123.11. |
| Appearance | Crystalline solid |
| Country of Origin | Made in India |
| Boiling Point | 357.4degC at 760 mmHg |
| CAS No | 98-96-4 |
| EINECS | 202-717-6 |
| Flash Point | 169.9degC |
| Formula | C5H5N3O |
We are offering high quality of Pyrazinamide Api Powder. We are known for manufacturing, exporting, distributing, trading and supplying Pyrazinamide Api Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Pyrazinamide Api Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Pyrazinamide Api Powder. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who are manufacturing Pyrazinamide Api Powder as well as Intermediates of Pyrazinamide Api Powder.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Pyrazinamide Api Powder to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.Pyrazinamide is an essential first-line anti-tuberculosis (TB) medication used in combination with other drugs for the treatment of Mycobacterium tuberculosis infections. It is a prodrug that is converted into its active form, pyrazinoic acid, within the bacterial cell, disrupting bacterial growth.Chemical Name: Pyrazine-2-carboxamide Molecular Formula: C₅H₅N₃O
Molecular Weight: 123.11 g/mol
CAS Number: 98-96-4 Appearance: White to pale yellow crystalline powder
Solubility: Soluble in water and ethanol, slightly soluble in ether
Melting Point: 189–192°C
Mechanism of Action:
Pyrazinamide is a prodrug that is activated by bacterial pyrazinamidase (PncA) to pyrazinoic acid (POA), which disrupts membrane potential and intracellular pH homeostasis in Mycobacterium tuberculosis, leading to bacterial cell death. It is most effective in acidic environments, making it especially useful against TB bacteria in macrophages and necrotic lung lesions.
Absorption: Well absorbed orally
Metabolism: Primarily metabolized in the liver to pyrazinoic acid
Excretion: Eliminated through urine (mainly as metabolites)
Half-life: 9–10 hours (may be prolonged in renal impairment)
Therapeutic Uses & Indications:
Treatment of active tuberculosis (TB)
Always used in combination with other TB drugs (e.g., rifampicin, isoniazid, ethambutol) to prevent drug resistance
Works effectively against dormant TB bacteria within acidic lesions
Dosage & Administration:
Adults:
Standard dose: 15–30 mg/kg per day (maximum 2 g/day)
Intermittent therapy (twice weekly): 50–70 mg/kg
Pediatric dosage: 15–30 mg/kg per day
Administration: Taken orally, usually once daily with food to reduce gastrointestinal side effects
Side Effects:Hepatotoxicity (most serious risk) – liver enzyme elevation, jaundice, hepatitisHyperuricemia (may cause gout attacks)Gastrointestinal disturbances – nausea, vomiting, loss of appetiteArthralgia (joint pain)Skin rash, photosensitivity
Contraindicated in:Severe liver disease Acute gout Patients with kidney impairment
Pregnant or breastfeeding women (only if benefits outweigh risks) Rifampicin & Isoniazid: Increased risk of liver toxicity
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Packaging Size | 25 Kg |
| Packaging Type | Drum |
| CAS Number | 38304 91 5 |
| Melting Point | 272-274degC (dec.)(lit.) |
| Density | 1.52 g/cm3 |
| Molecular Weight | 209.29 |
| Appearance | White crystalline powder |
| Boiling Point | 351.7degC at 760 mmHg |
| CAS No | 38304-91-5 |
| Deleted CAS | 16317-69-4 |
| EINECS | 253-874-2 |
| Flash Point | 166.5degC |
| Form | Powder |
| Formula | C9H15N5O |
| Risk Codes | 22-36/37/38-26/27/28 |
| Safety | 26-36-45-36/37/39-22 |
We are offering high quality of Minoxidil Api Powder.We are known for manufacturing, exporting, distributing, trading and supplying Minoxidil Api Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness. Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Minoxidil Api Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports. Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Minoxidil Api Powder. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Minoxidil Api Powder as well as Intermediates of Minoxidil Api Powder. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years. Shreeji Pharma International currently export Minoxidil Api Powder countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Minoxidil API (Active Pharmaceutical Ingredient)
General Information:
Chemical Name: 2,4-Pyrimidinediamine, 6-(1-piperidinyl)-, 3-oxide
Molecular Formula: C₉H₁₅N₅O
Molecular Weight: 209.25 g/mol
CAS Number: 38304-91-5
Synonyms: 6-(Piperidin-1-yl)pyrimidine-2,4-diamine 3-oxide
Physical and Chemical Properties:
Appearance: White to off-white crystalline powder
Solubility: Slightly soluble in water, soluble in propylene glycol and ethanol
Melting Point: 248–268°C
pH (1% solution): 6.0–7.5
Pharmacological Information:
Mechanism of Action: Minoxidil is a potassium channel opener that causes vasodilation, improving blood flow to hair follicles. It is primarily used for promoting hair growth and treating androgenetic alopecia (male and female pattern baldness).
Therapeutic Use: Topical minoxidil is used for hair regrowth, while oral minoxidil is used as an antihypertensive agent.
Absorption: When applied topically, less than 2% is systemically absorbed.
Metabolism: Primarily metabolized in the liver.
Excretion: Excreted mainly via the kidneys in urine.
Regulatory Status:
USP/BP/EP Compliance: Available in different grades meeting pharmacopoeial standards.
GMP Compliance: API manufacturing must follow Good Manufacturing Practices (GMP).
Drug Approvals: FDA, EMA, and other regulatory agencies approve minoxidil for hair loss treatment and hypertension.
Applications:
Topical Formulations: Used in 2%, 5%, and higher concentrations for hair regrowth solutions and foams.
Oral Formulations: Used at low doses (e.g., 2.5 mg, 5 mg) for treating hypertension and sometimes off-label for hair loss.
Storage & Stability:
Storage Conditions: Store in a cool, dry place at temperatures below 25°C.
Shelf Life: Typically 2–3 years under proper storage conditions.
Safety and Precautions:Side Effects: Possible scalp irritation, itching, redness (topical use); dizziness, hypotension, fluid retention (oral use).
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Composition | [Fe(OH)3(H2O)1.5]n [(C6H10O5)m]x |
| Color | Brownish red |
| CAS Number | 17099-81-9 |
| Usage | Commerical |
| Usage/Application | Pharma |
| Grade Standard | Pharma |
| Physical State | Powder |
| Type Of API | Raw |
| Purity | Carbohydrate Purity 26% to 34%,Polymaltose Purity 24% to 31% |
| Package Type | Drum |
| Model Number | 17099-81-9 |
| Chemical Name | Iron Hydroxide Polymaltose Complex,Iron Polymaltose |
| API Form | Powder |
We are offering high quality of Iron (III) Hydroxide Polymaltose Complex. We are known for manufacturing, exporting, distributing, trading and supplying Iron (III) Hydroxide Polymaltose Complex in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Iron (III) Hydroxide Polymaltose Complex in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Iron (III) Hydroxide Polymaltose Complex. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Iron (III) Hydroxide Polymaltose Complex as well as Intermediates of Iron (III) Hydroxide Polymaltose Complex is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Iron (III) Hydroxide Polymaltose Complex to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Iron (III) Hydroxide Polymaltose Complex (also known as Iron (III) Hydroxide Polymaltose Complex or Iron Polymaltose) is an iron-containing compound used primarily as an oral supplement for treating iron deficiency and iron deficiency anemia. It’s designed to provide iron in a less irritating and more bioavailable form than traditional ferrous iron salts (like ferrous sulfate). Here's a detailed breakdown of the complex:
1. Chemical Composition
The Iron (III) Hydroxide Polymaltose Complex is composed of:
Iron (III) Hydroxide (Fe(OH)₃): This is the iron core of the complex. Iron (III) refers to the ferric state of iron, where iron has a +3 oxidation state.
Polymaltose: Polymaltose is a carbohydrate polymer that is used to stabilize the iron ions in the complex. It is derived from maltose, a sugar that is typically found in plants and is created by linking multiple sugar units together. It helps improve the absorption and tolerance of iron in the gastrointestinal tract.
The complex consists of iron ions that are bound to a carbohydrate structure, which facilitates the controlled release of iron into the body while minimizing the adverse effects usually associated with iron supplements.
3. Clinical Uses
Iron (III) Hydroxide Polymaltose Complex is used as a treatment for:
Iron deficiency anemia (IDA): A condition in which the body does not have enough iron to produce hemoglobin, leading to symptoms like fatigue, weakness, and pallor.
Iron deficiency: It is used to restore adequate iron levels in individuals who have insufficient iron intake, poor absorption, or increased iron demand (e.g., during pregnancy or growth spurts).
4. Side Effects
While Iron (III) Hydroxide Polymaltose Complex is generally better tolerated than other iron supplements, there can still be some side effects:
Mild gastrointestinal discomfort: While less common than with other iron formulations, some people may still experience mild nausea, stomach cramps, or bloating.
Allergic reactions: Rarely, some individuals might have an allergic reaction to the complex, with symptoms like rash, itching, or swelling.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Shelf life | 5 years |
| CAS Number | 3506-09-0 |
| Melting Point | 163-165degC(lit.) |
| Solubility | H2O 50 mg/mL,clear,colorless |
| Molecular Weight | 295.8 |
| Country of Origin | Made in India |
| Formula | C16H22ClNO2 |
We are offering high quality of Propranolol Hcl. We are known for manufacturing, exporting, distributing, trading and supplying Propranolol Hcl in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Propranolol Hcl in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Propranolol Hcl. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Propranolol Hcl as well as Intermediates of Propranolol Hcl. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Propranolol Hcl to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Molecular Formula: C₁₆H₂₂ClNO₂
Molecular Weight: 295.8 g/mol
Chemical Structure: Propranolol HCl consists of a naphthalene ring system connected to a propanolamine side chain, with the hydrochloride salt enhancing its solubility.
Physical Appearance: White crystalline powder
Melting Point: 163–165°C
Solubility: Highly soluble in water (50 mg/mL)
Pharmacokinetics:
Absorption: Propranolol is almost completely absorbed orally; however, due to extensive first-pass hepatic metabolism, its bioavailability is reduced.
Distribution: Widely distributed throughout body tissues, including the lungs, liver, kidneys, heart, and brain. It crosses the blood-brain barrier and placenta and is excreted into breast milk.
Plasma Protein Binding: Approximately 90–95%, indicating a high affinity for plasma proteins.
Metabolism: Extensively metabolized by the liver, primarily via the cytochrome P450 enzyme system, particularly CYP2D6.
Elimination Half-Life:
Intravenous (IV) Administration: Initial phase of about 10 minutes; terminal phase approximately 2.3 hours.
Oral Administration: Half-life ranges from 3 to 6 hours with chronic administration.
Extended-Release Formulations: Apparent half-life of about 10 hours.
Excretion: Primarily excreted in urine, with at least eight metabolites identified. A small percentage (1–4%) of the drug is excreted unchanged in feces.
Storage Conditions:
Oral Forms: Store in tight, light-resistant containers at 20–25°C; protect from moisture, freezing, or excessive heat.
Parenteral Forms: Store at 20–25°C; protect from freezing or excessive heat.
Safety and Handling:
Hazard Statements: H302 (Harmful if swallowed), H332 (Harmful if inhaled), H317 (May cause an allergic skin reaction), H312 (Harmful in contact with skin).
Precautionary Statements: P261 (Avoid breathing dust/fume/gas/mist/vapors/spray), P280 (Wear protective gloves/protective clothing/eye protection/face protection).
Risk Codes: Xn (Harmful)
Safety Measures: Handle with appropriate safety measures, including the use of personal protective equipment to prevent inhalation, ingestion, or skin contact.
Compatibility:
Solution Compatibility: Compatible with Dextrose 5% in water, Dextrose 5% in sodium chloride 0.45% or 0.9%, Ringer’s injection (lactated), and Sodium chloride 0.45% or 0.9%.
Drug Compatibility: Compatible with Dobutamine HCl and Verapamil HCl.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Shelf life | 5 Years |
| Molecular Formula | C23H14O11.2Na |
| Country of Origin | Made in India |
| Application | Anti Asthamatic |
| CAS Number | 15826-37-6 |
| Synonyms | DSCG; intal; aarane; fpl670; nasmil; Nalcro; aararre; lomudal; lomudas; nalcrom |
We are offering high quality of Sodium Cromoglycate We are known for manufacturing,exporting, distributing, trading and supplying Sodium Cromoglycate in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier of Sodium Cromoglycate in Gujarat. India. Shreeji Pharma International manufacturing & supplying all products under GMP site with all types of regulatory supports.Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Sodium Cromoglycate Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Sodium Cromoglycate as well as Intermediates of Sodium Cromoglycate Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years. Shreeji Pharma International currently export Sodium Cromoglycate to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAMcountries, Central American Countries and in European countries
- Technical Specifications:
CAS Number: 15826-37-6
Name: 4H-1-Benzopyran-2-carboxylicacid, 5,5'-[(2-hydroxy-1,3-propanediyl)bis(oxy)]bis[4-oxo-, sodium salt (1:2)
Superlist Name: Sodium cromoglycate
Formula: C23H14Na2O11
Molecular Weight: 512.35
Synonyms: Aarane;Allergocrom;Altoderm;Colimune;Cromolyn disodium salt;Cromovet;DSCG;Disodium 1,3-bis(2-carboxy-5-chromonyloxy)-2-propanol;Disodium chromoglycate;
EINECS: 239-926-7
Melting Point: 241-242 °C
Boiling Point: 752.3 °C at 760 mmHg
Flash Point: 263.9 °C
Appearance: white crystalline powder
- Introduction of product:Disodium cromoglycate is an organic sodium salt that is the disodium salt of cromoglycic acid. It has a role as an anti-asthmatic drug and a drug allergen.
- How does it work?:Sodium cromoglicate eye drops relieve the symptoms of allergic conjunctivitis by reducing the release of a chemical called histamine which causes inflammation. They are suitable for use in adults and children.
- Applications. Or where it is used:The active ingredient Sodium Cromoglicate belongs to a group of medicines called anti-inflammatory/anti-allergy agents. Sodium Cromoglicate Eye Drops are used to treat red, watery, itchy eyes caused by allergies such as hayfever, house dust mites and pet hair.
- How to use:Sodium cromoglicate drops are used to treat red, watery, itchy eyes caused by allergies such as hay fever. Use the drops in both eyes - use one drop four times a day. Eye drops may cause blurred vision when first put in. Wait until this clears before you drive and before you use tools or machines
- Side effects:The following side effects have been reported by at least 1% of people taking this medication. Many of these side effects can be managed, and some may go away on their own over time.Coughing,stuffy nose,throat irritation or dryness,unpleasant taste, upset stomach
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Prescription/Non prescription | Prescription |
| Type of API | Digestive System API |
| Shelf life | 5 years |
| Molecular Weight | 350.862 g/mol |
| Country of Origin | Made in India |
| CAS ID | 66357-35-5 |
| EC Number | 266-333-0 |
| Formula | C13H22N4O3S |
We are offering high quality of Ranitidine HCL. We are known for manufacturing, exporting, distributing, trading and supplying Ranitidine HCL in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Ranitidine HCL in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Ranitidine HCL. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Ranitidine HCL as well as Intermediates of Ranitidine HCL. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.Shreeji Pharma International currently exports Ranitidine HCL to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.Ranitidine Hydrochloride (HCl) is a histamine-2 (H₂) receptor antagonist (H₂ blocker) used to reduce stomach acid production. It was widely prescribed for conditions like gastroesophageal reflux disease (GERD), peptic ulcers, Zollinger-Ellison syndrome, and acid indigestion. However, due to concerns over N-nitrosodimethylamine (NDMA) contamination, its use has been banned or restricted in several countries.Chemical Properties:Chemical Name: N-(2-[(5-[(Dimethylamino)methyl]furan-2-yl)methylthio]ethyl)-N'-methyl-2-nitroethene-1,1-diamine hydrochlorideMolecular Formula: C₁₃H₂₂N₄O₃S·HCl Molecular Weight: 350.87 g/molCAS Number: 66357-59-3 Appearance: White to pale yellow crystalline powderSolubility: Freely soluble in water, alcohol, and methanolMelting Point: ~140°C Stability: Sensitive to heat, light, and moistureMechanism of Action: Blocks histamine (H₂) receptors in the stomach, reducing acid secretion.Lowers basal and stimulated gastric acid production, aiding ulcer healing and reflux control.Absorption: Rapid, peak plasma concentration in 2–3 hours.Bioavailability: ~50% (due to first-pass metabolism). Metabolism: Metabolized in the liver (partial metabolism). Half-life: ~2–3 hours.Excretion: Primarily via urine (~30–40% unchanged). Therapeutic Uses & Indications: Gastroesophageal Reflux Disease (GERD)Peptic Ulcers (Duodenal & Gastric Ulcers)Zollinger-Ellison Syndrome (Hyperacid Secretion Disorder) Erosive Esophagitis Dyspepsia & Acid IndigestionDosage & Administration: Usual adult dose: 150 mg twice daily or 300 mg once daily (bedtime).Pediatric dose: 2–4 mg/kg/day, divided into two doses. Route: Oral tablets, syrup, injectable forms (IV/IM).Side Effects: Common: Headache, dizziness, diarrhea, constipation.Serious: Liver toxicity (elevated liver enzymes, jaundice).Blood disorders (thrombocytopenia, leukopenia – rare).CNS effects (confusion, hallucinations in elderly patients).NDMA Contamination Concerns:Potential carcinogenic risk led to market withdrawal in many regions.Precautions & Contraindications:Long-term users (risk of vitamin B12 deficiency). Pregnant & breastfeeding women (use only if necessary).Drug
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Packaging | Box |
| Usage/Aplication | Pharmaceutical |
| Color | skin color |
| Manufacturer | Shreeji phama |
| Country of Origin | Made in India |
We are offering high quality of Hydrocortisone Acetate Powder. We are known for manufacturing, exporting, distributing, trading and supplying Hydrocortisone Acetate Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Hydrocortisone Acetate Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Hydrocortisone Acetate Powder.
Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Hydrocortisone Acetate Powder as well as Intermediates of Hydrocortisone Acetate Powder.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Hydrocortisone Acetate Powder to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Hydrocortisone Acetate is a synthetic corticosteroid used in various pharmaceutical applications. It’s a derivative of hydrocortisone (cortisol), which is naturally produced by the adrenal glands and plays a key role in regulating inflammation, immune function, and other physiological processes.
Here are the technical details of hydrocortisone acetate:
1. Chemical Structure
IUPAC Name: 9α-Fluoro-11β,17α,21-trihydroxypregn-1,4-diene-3,20-dione
Molecular Formula: C21H30O6
Molar Mass: 374.47 g/mol
CAS Number: 50-03-3
Molecular Weight: 374.47 g/mol
CAS Number: 50-03-3
EINECS Number: 200-069-5
Hydrocortisone acetate is a derivative where an acetate ester group (–COOCH3) is attached to the hydroxyl group at the 21-position of hydrocortisone, increasing its potency and prolonging its effect when applied.
2. Physical Properties
Appearance: White to almost white, crystalline powder.
Solubility: Slightly soluble in water, freely soluble in alcohol, chloroform, and acetone.
3. Uses and Indications
Hydrocortisone acetate is primarily used to treat inflammatory and autoimmune conditions, as well as conditions where corticosteroid therapy is indicated:
Topical Use:
Treatment of skin conditions such as eczema, psoriasis, dermatitis, insect bites, and allergic skin reactions.
Used for inflammatory conditions in the skin or mucous membranes.
Injectable Form:
Relief of symptoms associated with joint inflammation, bursitis, and tendonitis.
Used to treat inflammation in the eye or other tissues requiring localized treatment.
Can be injected into the body (e.g., into joints) for conditions such as rheumatoid arthritis or osteoarthritis.
Oral Use (Less Common):
In some cases, hydrocortisone acetate is used in oral formulations to replace or supplement natural cortisol in patients with adrenal insufficiency.
4. Therapeutic Benefits
Hydrocortisone acetate is valued for its ability to reduce inflammation and control the immune system’s response. Some of the therapeutic benefits include:
Anti-inflammatory: Reduces swelling, redness, and irritation caused by inflammatory conditions.
Systemic Side Effects: When used in injectable or oral forms, potential side effects include:
Increased blood pressure.
Additional Information:
Product Details:
| Grade Standard | BP |
| Packaging Type | Drum |
| Melting Point | 255degC |
| Density | 1.614 g/cm3 |
| Solubility | DMSO soluble |
| Molecular Weight | 351.40 |
| Appearance | Light yellow solid |
| Country of Origin | Made in India |
| CAS No | 71125-38-7 |
| Deleted CAS | 133687-22-6 |
| Formula | C14H13N3O4S2 |
| Risk Codes | 22-36/37/38 |
| Safety | 26 |
We are offering high quality of Meloxicam Powder We are known for manufacturing, exporting, distributing, trading and supplying Meloxicam Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness. Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Meloxicam Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports. Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Meloxicam Powder .Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Meloxicam Powder as well as Intermediates of Meloxicam Powder .Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Meloxicam Powder countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.Meloxicam is a nonsteroidal anti-inflammatory drug (NSAID) commonly used to treat pain and inflammation. It’s often prescribed for conditions like arthritis, osteoarthritis, rheumatoid arthritis, and other inflammatory disorders. When used in powder form, meloxicam is typically intended for preparing oral solutions or suspensions.
Here’s a more detailed description of meloxicam powder:
General Information:
Class: Nonsteroidal anti-inflammatory drug (NSAID)
Uses: It’s mainly used to relieve symptoms of arthritis, such as pain, swelling, and stiffness. It may also be used to manage other types of inflammatory conditions.
Mechanism of Action: Meloxicam works by inhibiting the enzyme cyclooxygenase (COX), specifically COX-2, which is involved in the production of prostaglandins that cause inflammation, pain, and fever.
Formulation:
Meloxicam Powder: Typically, the powder is used to prepare a liquid suspension for oral administration. The powder may be mixed with a specific amount of water or another solvent to form a solution that can be easily consumed.
Concentration: The concentration of meloxicam powder varies depending on the intended formulation. Common oral dosages for meloxicam are 7.5 mg or 15 mg, but the amount may be adjusted based on specific treatment needs.
Dosage:The standard dosage for meloxicam is usually 7.5 mg to 15 mg once daily, but the exact dose can vary depending on the condition being treated, the patient's health history, and the doctor’s prescription.
Side Effects:
Common: Nausea, diarrhea, stomach pain, or headache.
Serious Risks: Long-term or high-dose use of meloxicam may increase the risk of cardiovascular problems (e.g., heart attack or stroke) and gastrointestinal issues (e.g., ulcers or bleeding). Kidney problems can also arise, especially in patients with preexisting conditions.
Not Recommended For: People with certain conditions, including active gastrointestinal bleeding, severe heart disease, or kidney impairment.
Interactions: Meloxicam can interact with other medications, such as blood thinners, other NSAIDs, certain antidepressants, and blood pressure medications.
General Information
Chemical Name: Meloxicam
Molecular Formula: C₁₄H₁₃N₃O₄S
Molecular Weight: 351.4 g/mol
CAS Number: 71125-38-7
Drug Class: Non-Steroidal Anti-Inflammatory Drug (NSAID)
Form: Fine yellowish powder
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Cas Number | 99-66-1 |
| Melting Point | 129-132 DegreeC |
| Shelf Life | 5 YEARS |
| Density | 0.926 g/cm3 |
| Solubility | Slightly soluble in water |
| Molecular Weight | 144.21 |
| Appearance | powder |
| Country of Origin | Made in India |
| Boiling Point | 220degC at 760 mmHg |
| Flash Point | 116.6degC |
| Risk Codes | 22-36/37/38-39/23/24/25-23/24/25-11 |
| Formula | C8H16O2 |
| EINECS | 202-777-3 |
| Safety | 26-45-36/37-16 |
We are offering high quality of Valproic Acid. We are known for manufacturing, exporting, distributing, trading and supplying Valproic Acid in in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Valproic Acid in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Valproic Acid. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Valproic Acid as well as Intermediates of Valproic Acid.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Valproic Acid to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Valproic Acid (also known as valproate) is a medication primarily used to treat a variety of neurological and psychiatric conditions. It is commonly used as an anticonvulsant, mood stabilizer, and in the treatment of other disorders. Here are the detailed descriptions and information about valproic acid:
General Information:
Chemical Name: 2-Propylpentanoic acid.
Molecular Formula: C8H16O2.
CAS Number: 99-66-1.
Other Names: Valproate, Valproic Acid Sodium, Sodium Valproate (the sodium salt form).
Drug Class: Anticonvulsants, mood stabilizers.
Appearance:
Form: Typically available as tablets, capsules, liquid form, and sometimes as an injectable solution.
Color: White to off-white crystalline powder (in pure form).
Odor: No significant odor.
Uses:
Valproic acid has multiple uses in the treatment of medical conditions, including:
Dosage and Administration:
The oral dosage of valproic acid varies based on the condition being treated, the patient’s age, and individual response to the drug.
Typical Adult Dosage for epilepsy:
Start with 10-15 mg/kg/day, divided into 2-3 doses, and gradually increase as needed.
The usual maintenance dose is 20-60 mg/kg/day.
For bipolar disorder, dosages may range from 750 mg to 3,000 mg per day.
Liquid formulations may be prescribed for easier dose adjustments, especially in children or patients who have difficulty swallowing pills.
Side Effects:
Common side effects include:
Gastrointestinal issues (nausea, vomiting, indigestion, abdominal pain).
Weight gain.
Tremors (especially at higher doses).
Hair loss (alopecia).
Drowsiness or sedation.
Dizziness or lightheadedness.
Liver toxicity: Can cause liver damage, especially in young children or those with preexisting liver conditions.
Serious side effects include:
Pancreatitis (inflammation of the pancreas).
Liver failure (rare but severe, especially in young children).
Severe allergic reactions, including rashes, fever, and swelling of the face or limbs.
Teratogenic effects: It is known to be harmful to a developing fetus and is contraindicated during pregnancy due to a significant risk of birth defects, particularly neural tube defects.
Storage:
Store at room temperature, away from moisture and light.
Keep medication in a tightly closed container.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Melting Point | 127-130degC |
| Density | 1.42 g/cm3 |
| Molecular Weight | 349.31047 [g/mol] |
| Appearance | Cyrstalline solid |
| Boiling Point | 508.6degC at 760 mmHg |
| CAS No | 137234-62-9 |
| Deleted CAS | 173967-54-9 |
| Flash Point | 261.4degC |
| Formula | C16H14F3N5O |
| Risk Codes | 22-36/38 |
| Safety | 26-36 |
We are offering high quality of Voriconazole. We are known for manufacturing, exporting, distributing, trading and supplying Voriconazole in in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Voriconazole in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Voriconazole. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Voriconazole as well as Intermediates of Voriconazole.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Voriconazole to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Voriconazole is an antifungal medication used to treat serious and life-threatening fungal infections. It belongs to the triazole class of antifungal agents and is known for its broad-spectrum activity against a variety of fungal pathogens. Voriconazole is typically used when infections are resistant to other antifungal treatments or when infections are severe.
General Information:
Chemical Name: (2R,3S)-2-(2,4-difluorophenyl)-5-fluoro-4-(1H-1,2,4-triazol-1-yl)pyrimidine.
Molecular Formula: C16H14F3N5.
CAS Number: 137234-62-9.
Brand Names: Vfend, among others.
Drug Class: Triazole antifungal.
Storage:
Oral Tablets/Suspension: Store at room temperature, away from moisture and light.
Intravenous Solution: Store at room temperature and protect from light.
Drug Interactions:
Voriconazole has several significant interactions due to its effect on the CYP450 enzyme system. Important drug interactions include:
Increased levels of other medications (e.g., cyclosporine, tacrolimus, phenytoin) due to reduced metabolism.
Reduced effectiveness of voriconazole when taken with strong CYP450 inducers like rifampin, carbamazepine, or phenytoin.
Increased risk of bleeding when combined with warfarin, requiring close monitoring of INR levels.
Visual Effects:
As visual disturbances are common during treatment, patients should be cautioned about engaging in activities requiring clear vision, such as driving.
Liver Function:
Patients with liver disease need careful monitoring as voriconazole can cause liver toxicity. Dose adjustments are necessary for those with mild to moderate hepatic impairment
Drug Interactions:
Voriconazole is metabolized by CYP450 enzymes, especially CYP2C19, CYP2C9, and CYP3A4. This means that it can interact with many other drugs metabolized by the same enzymes, such as phenytoin, warfarin, benzodiazepines, cyclosporine, and certain statins. Caution should be exercised, and dose adjustments may be required.
Additional Information:
Product Details:
| Grade Standard | USP |
| Grade | Pharma Grade |
| Packaging Size | 25Kg |
| Packaging | 25 Kg Bag |
| Purity | Greater than 99% |
| Usage/Application | Pharmaceutical |
| CAS Number | 51022-70-9 |
| Melting point | 157-158 Degree C |
| Boiling point | 433.5 Degree C |
| Molecular Weight | 239.311 g/mol |
| Chemical Formula | C13H21NO3 |
| Risk Codes | 43 |
| Solubility | Soluble in water |
| EINECS | 256-916-8 |
We are offering high quality of Salbutamol Sulfate We are known for manufacturing,exporting, distributing, trading and supplying Salbutamol Sulfate in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier of Salbutamol Sulfate in Gujarat. India. Shreeji Pharma International manufacturing & supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Salbutamol Sulfate Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Salbutamol Sulfate as well as Intermediates of Salbutamol Sulfate
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Salbutamol Sulfate to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAMcountries, Central American Countries and in European countries
Technical Specifications
SALBUTAMOL SULPHATE
CAS Number: 51022-70-9
Name: Albuterol sulfate
Formula: 2(C13H21NO3).H2O4S
Molecular Weight: 576.70
Deleted CAS: 36519-31-0
Synonyms: .alpha.1-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-.alpha., .alpha.-diol sulfate (2:1) salt;Bronchospray;(+-)-Salbutamol sulfate;Albuterol sulfate (USP);1-(4-Hydroxy-3-hydroxymethylphenyl)-2-(tert-butylamino)ethanol sulfate;Loftan;Epaq;1,3-Benzenedimethanol, alpha1-(((1,1-dimethylethyl)amino)methyl)-4-hydroxy-, sulfate (2:1) (salt) (9CI);Ventolin HFA;Emican;Salbutamol hemisulfate;Broncho Inhalat;Huma-Salmol;Albuterol sulfate / Salbutamol sulfate;
EINECS: 256-916-8
Melting Point: 180 °C
Boiling Point: 433.5 °C at 760 mmHg
Flash Point: 159.5 °C
Solubility: soluble in water
Appearance: white crystalline solid
Risk Codes: 43
Safety: 36/37
Introduction of product - Salbutamol is a drug used in the treatment of asthma, a chronic lung disease caused by inflammation of the lower airways.
How does it work - Salbutamol is used to relieve symptoms of asthma and chronic obstructive pulmonary disease (COPD) such as coughing, wheezing and feeling breathless. It works by relaxing the muscles of the airways into the lungs, which makes it easier to breathe. Salbutamol comes in an inhaler (puffer)
Applications. Or where it is used
Salbutamol is typically used to treat bronchospasm (due to any cause—allergic asthma or exercise-induced), as well as chronic obstructive pulmonary disease. It is also one of the most common medicines used in rescue inhalers (short-term bronchodilators to alleviate asthma attacks).
Manufacturing process -
The process comprises the steps that (1) chloromethylation reaction: reactants namely p-hydroxy benzaldehyde and paraformaldehyde react under an acidic condition to generate a compound 1; (2) hydrolysis reaction: the compound 1 is subjected to hydrolysis reaction under a weakly alkaline condition to generate a compound
Product Details:
| Minimum Order Quantity | 25 Kg |
| Form | Powder |
| Packaging Size | 50-200 kg |
| Packaging Type | Drum |
| Manufacturer | shreeji |
| Shelf Life | 5 years |
| Usage/Application | pharma use |
| Color | White |
| Country of Origin | Made in India |
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kilogram |
| Grade Standard | USP |
| Purity | Greater than 99% |
| Packaging Size | 25 Kg |
| Melting Point | 139degC |
| Density | 1.11 g/cm3 |
| Molecular Weight | 418.57 |
| Appearance | White powder |
| Boiling Point | 564.9degC at 760 mmHg |
| CAS No | 79902-63-9 |
| Flash Point | 184.8degC |
| Formula | C25H38O5 |
| Risk Codes | 36/37/38 |
| Safety | 26-36 |
We are offering high quality of Simvastatin. We are known for manufacturing, exporting, distributing, trading and supplying Simvastatin in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Simvastatin in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Simvastatin. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Simvastatin as well as Intermediates of Simvastatin.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Simvastatin to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Simvastatin is a prescription medication belonging to the class of drugs known as statins (HMG-CoA reductase inhibitors). It is commonly used to lower cholesterol levels and reduce the risk of cardiovascular diseases, including heart attacks and strokes. Lowering low-density lipoprotein (LDL) cholesterol (bad cholesterol). Increasing high-density lipoprotein (HDL) cholesterol (good cholesterol).
Reducing triglycerides (a type of fat in the blood).
Lowering the risk of heart attack, stroke, and other cardiovascular complications in individuals with high cholesterol, diabetes, or heart disease.
Mechanism of Action
Simvastatin works by inhibiting HMG-CoA reductase, an enzyme in the liver responsible for producing cholesterol. By blocking this enzyme, simvastatin helps decrease cholesterol production and increases the liver’s ability to remove LDL cholesterol from the blood.
Side Effects Headache ,Nausea Constipation or diarrhea ,Muscle pain or weakness
Dizziness
Drug Interactions
Avoid combining with strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin) as they increase simvastatin levels.
Be cautious when using other cholesterol-lowering drugs (e.g., fibrates).
Increased risk of side effects with alcohol or high doses of niacin.
Storage & Handling
Store at room temperature (20-25°C) in a dry place.
Keep away from moisture and direct sunlight.
Keep out of reach of children.
Conclusion Simvastatin is an effective medication for managing cholesterol and preventing heart disease. However, it should be used under medical supervision to minimize the risk of side effects and drug interactions. Regular blood tests and cholesterol monitoring are essential while on this medication
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Packaging | 25Kg Drum |
| CAS Number | 51803-78-2 |
| Grade | Pharma Grade |
| Chemical Formula | C13H12N2O5S |
| Molecular Weight | 308.31 g/mol |
| Usage/Application | Pharmaceutical |
| Melting Point | 140-146 DegreeC |
| Boiling Point | 442 degree celsius |
| Risk Codes | 22-36/37/38 |
| EINECS | 257-431-4 |
| Flash Point | 221.1degC |
We are offering high quality of Nimuslide Api . We are known for manufacturing, exporting, distributing, trading and supplying Nimuslide Api in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Nimuslide Api in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Nimuslide Api . Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Nimuslide Api as well as Intermediates of Nimuslide Api .
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Nimuslide Api to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Nimuslide API Powder refers to Nimesulide, an active pharmaceutical ingredient (API) in powder form. Nimesulide is a non-steroidal anti-inflammatory drug (NSAID) with analgesic, antipyretic, and anti-inflammatory properties. It is widely used for the treatment of pain, inflammation, and fever associated with various conditions such as arthritis, musculoskeletal disorders, and post-operative pain.
1. Chemical Information:Chemical Name: N-(4-Nitro-2-phenoxyphenyl) methanesulfonamide
Molecular Formula: C13H12N2O5S
Molecular Weight: 308.31 g/mol
CAS Number: 51803-78-2
Appearance: Yellowish crystalline powder
Solubility: Practically insoluble in water; soluble in organic solvents like ethanol and acetone
Melting Point: 140-146°C
2. Pharmacological Properties: Nimesulide works by selectively inhibiting Cyclooxygenase-2 (COX-2) enzyme, which reduces the production of prostaglandins, thereby alleviating pain, swelling, and fever.
Anti-inflammatory Effect:
Suppresses the release of inflammatory mediators, leading to reduced pain and swelling.
Analgesic Effect: Provides relief from mild to moderate pain caused by musculoskeletal disorders, dental pain, and post-operative pain.
Antipyretic Effect: Reduces fever by affecting prostaglandin synthesis in the hypothalamus.
3. Uses & Applications: Nimuslide API Powder is used in the formulation of tablets, capsules, suspensions, and topical gels for:
Osteoarthritis and rheumatoid arthritis
Acute pain (toothache, sprains, back pain)
Dysmenorrhea (menstrual pain)
Post-surgical pain management
Fever associated with infections
4. Dosage & Administration:100 mg twice daily after meals (as per physician's advice)
Children: Not recommended for children under 12 years
Topical: Applied as a gel on the affected area
Duration of Use: Short-term only (5-7 days max)
5. Side Effects & Precautions: Common Side Effects:Nausea, vomiting, Diarrhea, Skin rashes, Dizziness
Serious Side Effects:Liver toxicity (hepatotoxicity), Gastric ulcers or bleeding, Kidney damage
Precautions:Not for long-term use due to liver toxicity risk
Avoid in patients with liver disease, kidney disease, or gastrointestinal ulcers
Not recommended for pregnant or breastfeeding women
6. Storage & Stability: Store in a cool, dry place away from moisture and direct sunlight.Shelf Life: Usually 2-3 years when stored properly.7. Regulatory Status:Banned in some countries due to liver toxicity concerns.Approved for restricted use in some regions with dosage and duration limitations.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kilogram |
| Solubility | Soluble in Water, Insoluble in Organic solvent. |
| Loss On Drying | Not more than 10.0 % w/w |
| Zinc Content | Between 14 % to 16 % w/w |
| pH | Between 5.0 and 7.5 |
| Ascorbic Acid | etween 68% to 89% w/w |
| For Zinc | To comply the identification test |
Additional Information:
Product Details:
| Cas Number | 99-76-3 |
| Melting Point | 125-128degC(lit.) |
| Molecular Weight | 152.16 |
| Formula | C8H8O3 |
| Form | Powder |
| Appearance | White crystalline powder |
| Boiling Point | 265.5degC at 760 mmHg |
| Deleted CAS | 156291-94-0 |
| Density | 1.209 g/cm3 |
| EINECS | 202-785-7 |
| Flash Point | 116.4degC |
| Risk Codes | 36/37/38-20/21/22 |
| Safety | 26-36-24/25 |
We are offering high quality of Methylene Blue We are known for manufacturing, exporting, distributing, trading and supplying Methylene Blue in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness. Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Methylene Blue in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports. Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Methylene Blue. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Methylene Blue as well as Intermediates of Methylene Blue. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years. Shreeji Pharma International currently export Methylene Blue countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries
Methylene Blue: Detailed Description
General Information:
Chemical Name: Methylene Blue (MB)
IUPAC Name: 3,7-bis(Dimethylamino)phenothiazin-5-ium chloride
Molecular Formula: C₁₆H₁₈ClN₃S
Molar Mass: 319.85 g/mol
CAS Number: 61-73-4
Physical Properties:
Appearance: Dark green crystalline powder with a bronze-like luster
Solubility: Soluble in water and ethanol, forming a deep blue solution
Melting Point: 100-110°C (decomposes)
Odor: Odorless
Chemical Properties:
Acts as a redox indicator, changing color based on oxidation state
Exhibits antibacterial, antifungal, and antiparasitic properties
Can generate reactive oxygen species under light exposure (used in photodynamic therapy)
Uses and Applications:
1. Medical Uses:
Methemoglobinemia Treatment: Restores normal oxygen transport in cases of methemoglobinemia by reducing Fe³⁺ in hemoglobin to Fe²⁺.
Antimalarial Agent: Previously used for malaria treatment due to its ability to inhibit Plasmodium falciparum.
Urinary Antiseptic: Used for urinary tract infections (UTIs).
Neuroprotective Agent: Being studied for its role in treating neurodegenerative diseases like Alzheimer's and Parkinson’s.
Septic Shock Treatment: Helps in cases of vasodilatory shock by increasing blood pressure.
2. Laboratory and Scientific Uses:
Biological Staining: Used in microbiology and histology to stain cells and tissues.
Redox Indicator: Employed in oxidation-reduction experiments.
Electron Donor in Chemistry: Participates in electron transfer reactions.
3. Industrial Uses:
Dye for Textiles and Leather: Used in coloring fabrics and leathers.
Aquaculture Treatment: Used to treat fungal and bacterial infections in fish.
4. Veterinary Uses:
Used in animals to treat methemoglobinemia and parasitic infections.
Mechanism of Action:
Methemoglobinemia: Methylene blue acts as an electron carrier, reducing methemoglobin back to hemoglobin.
Antimicrobial Action: Generates reactive oxygen species that disrupt bacterial and parasitic cells.
Neurological Benefits: Enhances mitochondrial function and increases ATP production, potentially improving cognitive function.
Side Effects and Precautions:
Side Effects:
Nausea, vomiting
Headache, dizziness
Hypertension
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Shelf life | 5 years |
| Melting Point | 171-175degC |
| CAS Number | 21829-25-4 |
| Density | 1.271 g/cm3 |
| Solubility | Soluble in DMSO |
| Molecular Weight | 346.34 |
| Appearance | Yellow crystalline solid |
| Country of Origin | Made in India |
| Boiling Point | 475.3degC at 760 mmHg |
| Deleted CAS | 101539-70-2|101554-38-5 |
| EINECS | 244-598-3 |
| Flash Point | 241.2degC |
| Formula | C17H18N2O6 |
| Risk Codes | 22-36/37/38 |
| Safety | 26-36 |
We are offering high quality of Nifedipine Api Powder. We are known for manufacturing, exporting, distributing, trading and supplying Nifedipine Api Powder in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
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Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Nifedipine Api Powder. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who are manufacturing Nifedipine Api Powder as well as Intermediates of Nifedipine Api Powder.
Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently exports Nifedipine Api Powder to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Name: Nifedipine: CAS Number: 21829-25-4, Chemical Formula: C₁₇H₁₈N₂O₆, Molecular , Weight: 346.33 g/mol, Appearance: Yellow crystalline powder, Category: Calcium channel blocker (CCB), Usage: Used in the pharmaceutical industry as an active pharmaceutical ingredient (API) for the formulation of antihypertensive and anti-anginal drugs.
Chemical Properties
Melting Point: 172-174°C
Stability: Light-sensitive; should be stored in an airtight container away from light and moisture
pH: Neutral to slightly acidic
Nifedipine is a dihydropyridine calcium channel blocker that inhibits the influx of calcium ions through L-type calcium channels in vascular smooth muscle and cardiac muscle. This results in vasodilation, reduced peripheral resistance, and decreased myocardial oxygen demand.
Therapeutic Indications:
Treatment of hypertension (high blood pressure)
Management of chronic stable angina (chest pain)
Used in Raynaud’s phenomenon
Preterm labor (tocolytic agent in some cases)
Dosage Forms Prepared Using Nifedipine API:
Immediate-release tablets
Extended-release tablets/capsules
Oral solutions
Injectable forms (less common)
Manufacturing & Quality Standards
Purity: Usually ≥ 99%
Impurities: Controlled as per pharmacopeial standards (USP, BP, EP)
Regulatory Compliance: Meets the requirements of FDA, GMP, and other regulatory bodies
Packaging: Typically available in aluminum foil bags or fiber drums with polyethylene liners (1 kg, 5 kg, 25 kg sizes)
Storage Conditions:
Store in a cool, dry place at controlled room temperature (15-30°C)
Keep away from direct sunlight and moisture
Protect from strong oxidizing agents
Handling Precautions: Avoid inhalation and skin contact; use gloves and protective eyewear, Work in a well-ventilated area, Dispose of waste according to local regulations
Side Effects:
Common: Dizziness, headache, flushing, edema
Serious: Hypotension, tachycardia, allergic reactions
Contraindications:
Severe aortic stenosis
Unstable angina or recent myocardial infarction
Known hypersensitivity to dihydropyridine calcium channel blockers
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Strength | 2.5 mg |
| Pack Size | 10 Kg |
| Pack Type | Drum |
| Shelf life | 5 years |
| Melting Point | 246-248degC |
| CAS Number | 23031-32-5 |
| Formula | 2(C12H19NO3).H2SO4 |
| Country of Origin | Made in India |
| Appearance | Crystalline Powder |
| Boiling Point | 419.2degC at 760 mmHg |
| Deleted CAS | 98225-49-1 |
| EINECS | 245-386-3 |
| Flash Point | 165.3degC |
| Molecular Weight | 512.68 |
| Risk Codes | 42/43-63 |
| Safety | 26-36 |
We are offering high quality of Terbutaline Sulphate Powder. We are known for manufacturing, exporting, distributing, trading and supplying Terbutaline Sulphate Powder in in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Terbutaline Sulphate Powder in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Terbutaline Sulphate Powder. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who is manufacturing Terbutaline Sulphate Powder as well as Intermediates of Terbutaline Sulphate Powder.
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Shreeji Pharma International currently export Terbutaline Sulphate Powder to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Terbutaline Sulfate is a bronchodilator primarily used to treat respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). It is part of the beta-2 adrenergic agonist class, which works by relaxing the muscles in the airways, making it easier to breathe. Terbutaline Sulfate is available in different forms, including oral tablets, inhalers, and injectable solutions. Below is a detailed description of Terbutaline Sulfate.
Chemical Name:
(R)-1-(4-hydroxy-3,5-dimethylphenyl)-2-(tert-butylamino)ethanol sulfate
Molecular Formula:C12H19NO3•H2SO4
Molecular Weight:277.37 g/mol
CAS Number:23031-25-6 (Terbutaline Sulfate)
Description:
Terbutaline is a beta-2 adrenergic agonist, meaning it stimulates beta-2 adrenergic receptors found in the smooth muscle of the lungs. This leads to the relaxation of bronchial smooth muscle, causing bronchodilation (widening of the airways), which helps alleviate symptoms such as wheezing, shortness of breath, and chest tightness associated with asthma, COPD, and other similar conditions.
Terbutaline Sulfate is commonly used as a short-acting bronchodilator, providing quick relief from bronchospasm.
Physical Appearance:
Form: White to off-white crystalline powder.
Appearance in Solution: The injectable solution is clear and colorless.
Taste: The oral formulation may have a slightly bitter taste.
Solubility: Terbutaline sulfate is freely soluble in water and alcohol, and slightly soluble in chloroform.
Exercise-Induced Bronchoconstriction: It can be used to prevent or treat bronchospasm triggered by exercise.
Preterm Labor: Terbutaline is occasionally used off-label to relax uterine muscles and delay premature labor (although it is not widely recommended due to potential side effects).
Injectable Solution:
For acute bronchospasm or preterm labor, 0.25 mg is administered subcutaneously. The dose can be repeated after 20 minutes if necessary, but not more than 0.5 mg per hour.
For preterm labor, it is given at 0.25 mg every 20 minutes for up to 3 doses.
Storage:Oral Tablets: Store in a cool, dry place, away from light at room temperature (15–30°C or 59–86°F).
Inhalers: Store at room temperature and protect from heat or direct sunlight.
Injectable Solution: Store in a cool, dry place away from light. Do not freeze.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Grade Standard | USP |
| Purity | 99% |
| Molecular Weight | 331.35 |
| Melting Point | 198-200degC |
| Density | 1.563 g/cm3 |
| Appearance | Off-white to pale yellow solid |
| Country of Origin | Made in India |
| Available Forms | Powder |
| CAS No | 36322-90-4 |
| EINECS | 252-974-3 |
| Formula | C15H13N3O4S |
We are offering high quality of Piroxicam Api. We are known for manufacturing, exporting, distributing, trading and supplying Piroxicam Api in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Piroxicam Api in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
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Shreeji Pharma International currently exports Piroxicam Api to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Piroxicam is a nonsteroidal anti-inflammatory drug (NSAID) used as an active pharmaceutical ingredient (API) in medications that treat pain and inflammation. It is commonly prescribed for conditions such as arthritis (both osteoarthritis and rheumatoid arthritis) and other inflammatory disorders.
1. General Information:Chemical Name: Piroxicam
IUPAC Name: 4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
CAS Number: 36322-90-4, Molecular Formula: C₁₅H₁₃N₃O₄S, Molecular Weight: 331.35 g/mol
Therapeutic Category: Non-Steroidal Anti-Inflammatory Drug (NSAID)
Drug Type: API (Active Pharmaceutical Ingredient)
2. Physical & Chemical Properties: Appearance: Yellow crystalline powder
Solubility: Practically insoluble in water, soluble in ethanol, methanol, acetone, and slightly soluble in chloroform, Melting Point: 198°C - 202°C, pH: Slightly acidic
Stability: Stable under normal conditions; sensitive to light and moisture
3. Mechanism of Action: Piroxicam is a non-selective COX inhibitor that works by inhibiting cyclooxygenase enzymes (COX-1 and COX-2), reducing the synthesis of prostaglandins, which play a key role in inflammation, pain, and fever.
4. Uses and Applications: Treatment of osteoarthritis and rheumatoid arthritis
Management of musculoskeletal disorders, acute gout, and post-operative pain
Used as an anti-inflammatory, analgesic, and antipyretic agent
5. Pharmacokinetics: Absorption: Well absorbed after oral administration, Bioavailability: ~100%
Peak Plasma Concentration: 3 - 5 hours
Half-life: 30 - 60 hours (long-acting NSAID)
Metabolism: Primarily in the liver by hydroxylation
Excretion: Excreted mainly in urine and feces
6. Side Effects: Gastrointestinal irritation (gastritis, ulcers), Nausea, vomiting, dyspepsia, Renal impairment with prolonged use, Skin reactions (rash, photosensitivity), Increased cardiovascular risks (hypertension, thrombosis)
7. Precautions & Warnings: Avoid in patients with peptic ulcer disease, severe renal or hepatic impairment, Use with caution in elderly patients due to increased risk of GI and cardiovascular complications, Not recommended during pregnancy (especially in the third trimester) or breastfeeding
8. Storage Conditions: Store in a cool, dry place away from direct sunlight
Keep in well-closed containers, Recommended storage temperature: 15°C - 25°C
9. Regulatory & Quality Standards: Complies with USP, BP, EP, and IP standards
Should be tested for purity, assay, impurities, and dissolution
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Strength | 100 mg/5 ml |
| Brand | Shreeji |
| Shelf life | 5 Years |
| Country of Origin | Made in India |
| CAS No | 6493-05-6 |
| Density | 1.31 g/cm3 |
| EINECS | 229-374-5 |
| Flash Point | 275.1degC |
| Formula | C13H18N4O3 |
| Appearance | White to off-white solid |
| Boiling Point | 531.3degC at 760 mmHg |
| Molecular Weight | 278.35 |
We are offering high quality of Pentoxifylline. We are known for manufacturing, exporting, distributing, trading and supplying Pentoxifylline in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Pentoxifylline in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.Shreeji Pharma International is the largest manufacturer, Exporter and supplier of Pentoxifylline. Nowadays Shreeji Pharma International is one of the leading manufacturer and exporter, who are manufacturing Pentoxifylline as well as Intermediates of Pentoxifylline. Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.Shreeji Pharma International currently exports Pentoxifylline to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
1. General Information: Chemical Name: Pentoxifylline, IUPAC Name: 1-(5-Oxohexyl)-3,7-dimethylxanthine, CAS Number: 6493-05-6, Molecular Formula:,C<sub>13</sub>H<sub>18</sub>N<sub>4</sub>O<sub>3</sub>, Molecular Weight: 278.31 g/mol, Appearance: White to off-white crystalline powder, Solubility: Freely soluble in dimethylformamide, slightly soluble in water and ethanol(2). Pharmacological Profile: Mechanism of Action: Pentoxifylline is a hemorheologic agent that improves blood flow by increasing red blood cell flexibility, reducing blood viscosity, and decreasing platelet aggregation. It also has anti-inflammatory and immunomodulatory properties.,Therapeutic Uses: Treatment of peripheral arterial disease (PAD) and intermittent claudication, Cerebrovascular disorders, Diabetic microangiopathy. (3). Specifications (Pharma Grade)
|
Parameter |
Specification |
|
Appearance |
White to off-white crystalline powder |
|
Identification |
Conforms to standard reference |
|
Assay (Purity) |
≥ 98.5% (HPLC or titration) |
|
Water Content |
≤ 0.5% (Karl Fischer method) |
|
Residue on Ignition |
≤ 0.1% |
|
Heavy Metals |
≤ 10 ppm |
|
Related Substances |
≤ 0.5% (by HPLC) |
|
pH (1% Solution) |
5.5 - 7.5 |
|
Melting Point |
104 - 107°C |
|
Specific Optical Rotation |
Not applicable |
(4). Manufacturing & Quality Standards: Pharmacopoeial Compliance: United States Pharmacopeia (USP), British Pharmacopoeia (BP), European Pharmacopoeia (EP), Indian Pharmacopoeia (IP) (5). Stability & Storage Conditions: Store in a cool, dry place away from direct sunlight, Keep at temperatures below 25°C, Protect from moisture and air exposure,Shelf Life: 3-5 years when stored under recommended conditions (6). Safety & Handling, Toxicity: Generally well-tolerated; adverse effects include dizziness, nausea, headache, and gastrointestinal discomfort., Precautions: Avoid use in patients with severe bleeding disorders, Not recommended for use during pregnancy unless necessary
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kg |
| Prescription/Non prescription | Non prescription |
| Type of API | Anti Infective API |
| CAS Number | 557-68-6 |
| Shelf life | 5 years |
| Form | Powder |
| Purity/Concentration | 99.9% |
| Brand Name | shreeji |
| pH Value | 5.5~7.5 |
| Packaging Size | 25Kgs |
| Solubility | It is easily soluble in water |
| Molecular Weight | 509.69 |
| Assay | 97.0~102.0 |
| Molecular Formula | C12H22O14Zn |
| Country of Origin | Made in India |
We are offering high quality of Zinc Gluconate. We are known for manufacturing, exporting, distributing, trading and supplying Zinc Gluconate in in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Zinc Gluconate in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
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Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Zinc Gluconate to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Zinc Gluconate is a common and widely used form of zinc supplement. It is a compound consisting of zinc and gluconic acid, a naturally occurring organic acid that is derived from glucose. Zinc gluconate is commonly used in dietary supplements due to its bioavailability, which makes it effective for addressing zinc deficiencies and supporting overall health.
1. Chemical Structure:
IUPAC Name: Zinc gluconate
Molecular Formula: C6H12O7Zn\text{C}_6 \text{H}_{12} \text{O}_7 \text{Zn}C6H12O7Zn
Molar Mass: Approximately 455.8 g/mol
Structure: Zinc gluconate consists of zinc (Zn²⁺) ions bound to gluconate, which is the conjugate base of gluconic acid (a product of glucose metabolism). The gluconate molecule helps stabilize the zinc ion and facilitate its absorption in the digestive system.
. Benefits of Zinc Gluconate:
Zinc is an essential mineral with numerous critical roles in the body. Zinc gluconate provides a well-tolerated, effective source of zinc for individuals needing to boost their zinc levels.
Key Health Benefits:
Immune System Support: Zinc plays a crucial role in immune function by helping maintain the proper development and function of immune cells, including T-cells and macrophages. Zinc gluconate helps bolster the immune system, making it an essential supplement during cold and flu seasons.
Wound Healing: Zinc is involved in cell division and tissue growth, making it important for wound healing and tissue repair. Zinc gluconate supports the healing of minor wounds, cuts, and burns.
Skin Health: Zinc gluconate is often used in the treatment of acne, dermatitis, and other skin conditions due to zinc’s ability to reduce inflammation, regulate oil production, and promote cell turnover.
Cognitive Function: Zinc is vital for brain health, influencing neurotransmitter function, synaptic plasticity, and cognitive performance. Zinc gluconate supports mental clarity, focus, and memory.
Hormonal Balance: Zinc is involved in the regulation of various hormones, including insulin, thyroid hormones, and reproductive hormones. Zinc gluconate can help balance these hormones, contributing to overall health and well-being.
Storage: Zinc gluconate supplements should be stored in a cool, dry place, away from heat, moisture, and direct sunlight. Proper storage will help maintain the potency and effectiveness of the supplement.
Additional Information:
Product Details:
| Minimum Order Quantity | 25 Kilogram |
| Molecular Weight | 166.19 |
| Melting Point | 300degC |
| CAS Number | 1069-66-5 |
| Solubility | Water 50 mg/mL |
| Appearance | White solid |
| Country of Origin | Made in India |
| EINECS | 213-961-8 |
| Flash Point | 116.6degC |
| Formula | C8H15NaO2 |
| Boiling Point | 220degC at 760 mmHg |
| Risk Codes | 22-61-36/38-36/37/38 |
We are offering high quality of Sodium Valproate. We are known for manufacturing, exporting, distributing, trading and supplying Sodium Valproate in Gujarat, India. Further, this is safely packaged by our professionals in diverse packaging options that maintain its purity and effectiveness.
Shreeji Pharma International is leading Manufacturer, Exporter, Distributor, and Supplier Sodium Valproate in Gujarat. India. Shreeji Pharma International manufacturing & gmp; supplying all products under GMP site with all types of regulatory supports.
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Shreeji Pharma International is exporter, supplier, distributor and manufacturers of the Active Pharmaceuticals Ingredients in many countries for many years.
Shreeji Pharma International currently export Sodium Valproate to countries like Gulf Countries, South East Asia countries, African Countries, CIS Countries, LATAM countries, Central American Countries and in European countries.
Chemical Name: Sodium 2-propylpentanoate
Common Name: Sodium Valproate
Molecular Formula: C₈H₁₅NaO₂
Molecular Weight: ~166.19 g/mol
CAS Number: 1069-66-5
Appearance: White crystalline powder
Solubility: Highly soluble in water and alcohol
pH (1% solution): 7.0 – 8.5
Description & Uses
Sodium Valproate is a sodium salt of Valproic Acid, primarily used as an anticonvulsant and mood stabilizer in the treatment of epilepsy, bipolar disorder, and migraine prophylaxis. It works by increasing gamma-aminobutyric acid (GABA) levels in the brain, reducing nerve excitability.
Applications
pilepsy Treatment: Used for treating various types of seizures, including generalized, partial, and absence seizures.
Bipolar Disorder: Acts as a mood stabilizer to manage manic episodes. Migraine Prevention: Prescribed for chronic migraine prophylaxis.
Neuroprotective Effects: Studied for neurological disorders like Alzheimer's and Parkinson's disease.
Safety & Precautions
Dosage: Must be taken as prescribed by a physician (varies by condition and patient weight).
Side Effects: May include nausea, drowsiness, weight gain, hair loss, and liver function abnormalities.
Contraindications:
Pregnancy (Risk of birth defects)
Liver disease & pancreatic disorders
Hypersensitivity to valproates
Drug Interactions: Can interact with anticoagulants, antiepileptics, and some antidepressants.
Purity & Quality Standards
Pharmaceutical-Grade Purity: ≥ 98.0% (as per USP, EP, BP standards)
Moisture Content: ≤ 1.0%
Heavy Metals (Lead, Arsenic, etc.): ≤ 10 ppm
Residual Solvents: Must comply with ICH Q3C guidelines
Additional Information: