Furosemide BP API with COA

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Product Details:

Taste Bitter
Appearance White to slightly yellow crystalline powder
CAS No 54-31-9
EINECS No 200-210-6
Grade BP (British Pharmacopoeia)
Smell Odorless
Product Type Active Pharmaceutical Ingredient (API)
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Furosemide BP API with COA Price And Quantity

Minimum Order Quantity 25 Kilograms

Furosemide BP API with COA Product Specifications

Appearance White to slightly yellow crystalline powder
Taste Bitter
CAS No 54-31-9
EINECS No 200-210-6
Grade BP (British Pharmacopoeia)
Smell Odorless
Product Type Active Pharmaceutical Ingredient (API)
Ingredients Furosemide (BP grade)
Solubility Slightly soluble in water, soluble in dilute alkali, alcohol, acetone, and ether
Refractive Rate Not listed
Poisonous No (when handled at recommended conditions)
Shape Crystalline
Molecular Weight 330.74 g/mol
Properties Odorless, white to slightly yellow crystalline powder, stable under recommended storage conditions
Storage Store in tightly closed container, protected from light, at room temperature (15-30C)
Shelf Life 5 years (if stored as per storage conditions)
Melting Point 205-210C (decomposition)
Physical Form Powder
HS Code 29420090
Purity 99.2% (as per COA)
Usage Used in the formulation of tablets and injectables for the treatment of edema and hypertension
Application Pharmaceutical manufacturing, mainly as a diuretic
Molecular Formula C12H11ClN2O5S
Density 1.7 Gram per cubic centimeter(g/cm3)
Ph Level Neutral aqueous solution
Structural Formula See referenced COA/image

Chloride Content Complies (max. 0.018%)
Heavy Metals Less than 10 ppm
Assay (on dried basis) 99.2% (98.5% - 101.0% as per BP)
Related Substances (Total Impurities) Not more than 0.5%
Loss on Drying 0.13% (max. 0.5%)
Packaging 25 kg HDPE drums / customized packaging
COA (Certificate of Analysis) Provided with each batch
Residue on Ignition 0.08% (max. 0.1%)
Sulphated Ash 0.05% (max. 0.1%)
Microbial Limits Complies with BP standard (Total aerobic microbial count: NMT 1000 CFU/g, Total yeast & mould: NMT 100 CFU/g)
Bacterial Endotoxins Complies with BP limit
Identification (IR) Complies with BP standard

Furosemide BP API with COA Trade Information

FOB Port ALL india and export
Payment Terms Cash Advance (CA), Cash in Advance (CID)
Supply Ability 1000 Kilograms Per Week
Delivery Time 7 Days
Sample Available Yes
Sample Policy Contact us for information regarding our sample policy
Main Export Market(s) Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
Main Domestic Market All India

Product Description

Furosemide is a potent loop diuretic (water pill) used to treat fluid retention (edema) and high blood pressure, often sold under the brand name Lasix. It works by enabling the kidneys to remove excess water and sodium from the body through increased urination.

Pharmaceutical-Grade Quality and Compliance

Furosemide BP API strictly adheres to British Pharmacopoeia (BP) standards, making it highly suitable for regulated pharmaceutical manufacturing. The product's comprehensive Certificate of Analysis details rigorous tests for identification, purity, microbial load, and other key quality parameters to ensure unmatched safety and efficacy for end users.

Versatile Usage in Drug Formulation

Primarily employed in the formulation of diuretic tablets and injectables, Furosemide BP is trusted for its consistent bioactivity and high purity. Its stable, odorless, and crystalline powder form allows easy integration into various pharmaceutical processes, supporting efficient production for both large- and small-scale manufacturers.

Safe and Secure Packaging for Extended Shelf Life

Supplied in robust 25 kg HDPE drums or customizable containers, Furosemide BP maintains its stability and quality during storage and transportation. The product remains effective for up to five years when stored at room temperature (15-30C), away from light and moisture, protecting your investment and ensuring safe availability for extended periods.

FAQ's of Furosemide BP API with COA:

Q: How is Furosemide BP API compliant with quality standards?

A: Furosemide BP API complies with British Pharmacopoeia (BP) standards for identification, purity, impurity profile, and microbial safety. Each batch is accompanied by a Certificate of Analysis (COA), ensuring conformity to all BP quality requirements.

Q: What is the typical use of Furosemide BP API in pharmaceuticals?

A: This API is primarily used in manufacturing tablets and injectables for the treatment of edema and hypertension. Its high purity and stability make it suitable for formulation in various dosage forms.

Q: When should Furosemide BP API be used during the manufacturing process?

A: Furosemide BP API is utilized at the active pharmaceutical ingredient (API) stage, during the compounding or blending processes, prior to the final drug product formulation in tablet or injectable form.

Q: Where is Furosemide BP API sourced and how is it packaged?

A: This API is manufactured and sourced in India, packaged in secure 25 kg HDPE drums, with customized packaging options available to meet specific logistic or storage requirements.

Q: What are the recommended storage conditions for Furosemide BP API?

A: It should be stored in tightly closed containers, protected from light, and kept at room temperature (15-30C). These conditions preserve its stability and extend its effective shelf life up to 5 years.

Q: How does the provided COA benefit pharmaceutical manufacturers?

A: The Certificate of Analysis (COA) verifies that the supplied API meets stringent BP quality parameters, such as purity, impurities, and microbial limits. This documentation supports regulatory compliance and ensures batch-to-batch consistency.

Q: What are the advantages of using Furosemide BP API with high purity and compliance?

A: High purity and strict BP compliance reduce the risk of contamination, support effective formulations, and contribute to the safety and therapeutic efficacy of the final pharmaceutical products.

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