Send Inquiry

Request To Call Back

Furosemide BP API with COA

Price 1 INR/ Kilograms

Get a Price/Quote

MOQ : 25 Kilograms

Furosemide BP API with COA Specification

Ph Level
Neutral aqueous solution

Molecular Formula
C12H11ClN2O5S

Purity
99.2% (as per COA)

EINECS No
200-210-6

HS Code
29420090

Density
1.7 Gram per cubic centimeter(g/cm3)

Taste
Bitter

Application
Pharmaceutical manufacturing, mainly as a diuretic

CAS No
54-31-9

Molecular Weight
330.74 g/mol

Structural Formula
See referenced COA/image

Shelf Life
5 years (if stored as per storage conditions)

Smell
Odorless

Physical Form
Powder

Refractive Rate
Not listed

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)

Appearance
White to slightly yellow crystalline powder

Product Type
Active Pharmaceutical Ingredient (API)

Melting Point
205-210C (decomposition)

Grade
BP (British Pharmacopoeia)

Shape
Crystalline

Solubility
Slightly soluble in water, soluble in dilute alkali, alcohol, acetone, and ether

Ingredients
Furosemide (BP grade)

Usage
Used in the formulation of tablets and injectables for the treatment of edema and hypertension

Residue on Ignition
0.08% (max. 0.1%)

Chloride Content
Complies (max. 0.018%)

COA (Certificate of Analysis)
Provided with each batch

Assay (on dried basis)
99.2% (98.5% - 101.0% as per BP)

Bacterial Endotoxins
Complies with BP limit

Packaging
25 kg HDPE drums / customized packaging

Identification (IR)
Complies with BP standard

Loss on Drying
0.13% (max. 0.5%)

Sulphated Ash
0.05% (max. 0.1%)

Related Substances (Total Impurities)
Not more than 0.5%

Microbial Limits
Complies with BP standard (Total aerobic microbial count: NMT 1000 CFU/g, Total yeast & mould: NMT 100 CFU/g)

Heavy Metals
Less than 10 ppm

Furosemide BP API with COA Trade Information

Minimum Order Quantity
25 Kilograms

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

About Furosemide BP API with COA

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.

Tell us about your requirement