Active Pharmaceutical Ingredient

Degarelix API Manufacturer & Supplier in India

Also known as: Firmagon

CAS: 214766-78-6 Oncology / GnRH Antagonist USP / BP / IP / EP Bulk Supply Available
Degarelix API Manufacturer India | Mediocon Inc
Degarelix — Pharmaceutical Grade API

Product Overview

CAS No: 214766-78-6  |  MF: C₈₂H₁₀₃ClN₁₈O₁₆  |  MW: 1632.29 g/mol

Degarelix is a synthetic peptidic gonadotropin-releasing hormone (GnRH) receptor antagonist used for the treatment of advanced hormone-sensitive prostate cancer. It rapidly reduces testosterone to castrate levels without initial testosterone surge seen with GnRH agonists. Mediocon Inc supplies pharmaceutical-grade Degarelix meeting IP, BP, EP, and USP standards.

Key Features

  • Analgesic, antipyretic & anti-inflammatory
  • USP/BP/IP compliant quality
  • Widely used in cardiovascular therapy
  • Suitable for tablet and effervescent formulations

Applications

  • Advanced hormone-sensitive prostate cancer
  • Androgen deprivation therapy (ADT)
  • Pre-surgical testosterone reduction
  • Prostate cancer clinical research

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 NameDegarelix
Also Known AsFirmagon
CAS Number214766-78-6
Molecular FormulaC₈₂H₁₀₃ClN₁₈O₁₆
Molecular Weight1632.29 g/mol
CategoryGnRH Receptor Antagonist / Antineoplastic
AppearanceWhite Lyophilized Powder
GradeUSP / BP / IP / EP

Analytical Specifications

ParameterSpecification
Assay99.0% Min.
Loss on DryingNMT 1.0%
Melting PointN/A (peptide)
Heavy MetalsComplies
pHN/A
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
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 Degarelix (CAS 214766-78-6) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Degarelix 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 — Degarelix API

What is the minimum order quantity for Degarelix API?
Mediocon Inc supplies Degarelix 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 Degarelix does Mediocon supply?
We supply Degarelix conforming to USP / BP / IP / EP 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 Degarelix API?
Every shipment of Degarelix 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 Degarelix bulk orders?
Standard lead time for Degarelix 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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