Allopurinol IP/BP/USP

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Allopurinol IP/BP/USP Specification

Origin of Medicine
Allopathic

Indication
Chronic gout, uric acid kidney stones, chemotherapy-induced hyperuricemia

Dosage Form
Powder

Salt Composition
Allopurinol IP/BP/USP

Pacakaging (Quantity Per Box)
As per customer requirement

Drug Type
Medicine Raw Material

Ingredients
Allopurinol

Physical Form
Powder

Function
Reduces uric acid synthesis

Recommended For
Gout, Hyperuricemia treatment

Dosage
As directed by physician

Dosage Guidelines
As per prescription

Suitable For
Adults

Quantity
500 gm, 1 kg, 5 kg, 25 kg

Allopurinol IP/BP/USP Trade Information

FOB Port
All Indian Port

Payment Terms
Telegraphic Transfer (T/T), Western Union

Delivery Time
7 Days

Sample Available
Yes

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
As Per Standard Packing

Main Export Market(s)
Australia, North America, Eastern Europe, Western Europe, Middle East, Africa, Central America, South America, Asia

Certifications
COA, MSDS

About Allopurinol IP/BP/USP

Allopurinol is a medication used to decrease high blood uric acid levels. It is specifically used to prevent gout, prevent specific types of kidney stones, and for the high uric acid levels that can occur with chemotherapy. It is taken by mouth or injected into a vein.

Name:Allopurinol
Synonyms:4-Hydroxypyrazolopyrimidine; 1H-Pyrazolopyrimidin-4-ol; HPP
Molecular Formula:C5H4N4O
Molecular Weight:136.11
CAS NO:315-30-0
Melting point:350 ºC
Water solubility:0.35 g/L (25 ºC)
Physical and Chemical Properties: White or white powder, insoluble in water.
Usage: This product can inhibit the production of uric acid, decreased serum uric acid concentration

Packaging details:

Packaging details:	25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.
Storage:	Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat
Shelf Life:	5 years if sealed and store away from direct sun light.

Superior Purity and Quality Assurance

Our Allopurinol IP/BP/USP is manufactured to achieve a purity of at least 99%, ensuring consistent pharmaceutical quality. Each batch is stringently tested for assay, physical characteristics, and compliance with international standards, making it ideal for use in high-quality pharmaceutical formulations.

Applications and Therapeutic Indications

Ideal for pharmaceutical formulation and API manufacturing, our Allopurinol powder is primarily indicated for the treatment of chronic gout, hyperuricemia, and uric acid kidney stones. Its function is to reduce uric acid synthesis, helping manage and prevent complications associated with excess uric acid levels.

Handling, Storage, and Shelf Life

To maintain optimum potency, store Allopurinol in a cool, dry environment away from direct sunlight. The product remains stable for up to three years when kept in recommended conditions. Its non-hazardous nature under normal use contributes to safer handling throughout the supply chain.

FAQs of Allopurinol IP/BP/USP:

Q: How should Allopurinol IP/BP/USP be stored for maximum stability?

A: Allopurinol should be stored in a cool, dry space, away from heat and sunlight. This ensures the product remains effective for up to three years. Always keep the packaging tightly sealed to protect against moisture and contamination.

Q: What is the primary use of Allopurinol IP/BP/USP in pharmaceutical manufacturing?

A: This product is chiefly used as an active pharmaceutical ingredient (API) in medicines aimed at reducing uric acid production. Commonly, it is included in formulations to manage chronic gout, hyperuricemia, uric acid kidney stones, and for patients undergoing chemotherapy.

Q: When should Allopurinol powder be administered?

A: Allopurinol is given according to a healthcare professionals direction, based on the individuals condition. It is typically prescribed for ongoing control of elevated uric acid and should be used as per the recommended dose and guidelines from a physician.

Q: Where is this pharmaceutical-grade Allopurinol produced and supplied from?

A: Our Allopurinol IP/BP/USP is manufactured and exported from India, adhering to IP/BP/USP specifications and global quality assurances for pharmaceutical raw materials.

Q: What is the process for using Allopurinol in medication formulation?

A: Allopurinol is incorporated as a raw powder during the drug manufacturing process. It is precisely weighed, blended, and refined according to pharmaceutical formulation guidelines to ensure the correct dosage and purity in the final medicine.

Q: What are the benefits of choosing high-purity Allopurinol for formulation?

A: Using Allopurinol with a minimum 99% purity ensures consistent efficacy, minimal impurities, and reliable therapeutic outcomes in finished pharmaceuticals, supporting better patient safety and predictable results.

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