Active Pharmaceutical Ingredient

Furosemide API Manufacturer & Supplier in India

Also known as: Lasix (brand)

CAS: 54-31-9 Loop Diuretic IP / BP / USP Bulk Supply Available
Furosemide API Manufacturer India | Mediocon Inc
Furosemide — Pharmaceutical Grade API

Product Overview

CAS No: 54-31-9  |  MF: C₁₂H₁₁ClN₂O₅S  |  MW: 330.74 g/mol

Furosemide is a potent loop diuretic that inhibits the Na-K-Cl co-transporter (NKCC2) in the thick ascending limb of the loop of Henle. It is used for the management of edema associated with congestive heart failure, liver cirrhosis, renal disease, and hypertension.

Mediocon Inc manufactures Furosemide IP/BP/USP as a high-purity active pharmaceutical ingredient for oral and injectable formulation manufacturers worldwide. Our Furosemide is produced under strict GMP conditions with full pharmacopoeial quality testing.

Key Features

  • Potent NKCC2 loop diuretic
  • Suitable for oral & injectable formulations
  • Fast-acting diuresis mechanism
  • GMP-certified pharmaceutical grade

Applications

  • Congestive heart failure edema management
  • Renal disease edema formulations
  • Hypertension combination therapies
  • Injectable diuretic product manufacturing

Why Choose Mediocon

  • ISO 9001:2015 & GMP certified manufacturing
  • Consistent batch-to-batch quality with full CoA
  • Export-ready documentation: COO, MSDS, DMF
  • Flexible MOQ for both R&D and commercial scale
  • Dedicated QA support for regulatory filings

Product Specifications

Product NameFurosemide
CAS Number54-31-9
Molecular FormulaC₁₂H₁₁ClN₂O₅S
Molecular Weight330.74 g/mol
CategoryLoop Diuretic
AppearanceWhite to Off-White Crystalline Powder
GradeIP / BP / USP
Packaging25 kg HDPE Drums / Aluminium Bags
StorageCool, Dry & Ventilated Place

Analytical Specifications

ParameterSpecification
AssayNLT 98.0% & NMT 101.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 10 ppm
Residual SolventsComplies ICH Q3C
Microbial LimitsComplies
IdentificationIR & UV Compliant
Melting Point206 – 210 °C
Packing25 kg HDPE drums / as per requirement

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Furosemide (CAS 54-31-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Furosemide is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Furosemide API

What is the minimum order quantity for Furosemide API?
Mediocon Inc supplies Furosemide with a minimum order quantity of 1 kg (sample packs available for R&D). We accommodate both small R&D quantities and large commercial-scale orders. Contact our sales team at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Furosemide does Mediocon supply?
We supply Furosemide conforming to IP / BP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis. Custom specifications can be accommodated for regulated markets.
What documentation is provided with Furosemide API?
Every shipment of Furosemide comes with: Certificate of Analysis (CoA), MSDS/SDS, Certificate of Origin (COO), and Drug Master File (DMF) support on request. We also provide GMP certification, ISO 9001:2015 compliance documentation, and full regulatory support for filings in USA (FDA), Europe (EMA), and other markets.
What is the lead time and shipping for Furosemide bulk orders?
Standard lead time for Furosemide is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging (25 kg HDPE drums / aluminium foil bags). All shipments include temperature-controlled logistics options where required by the product's storage conditions.
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