Active Pharmaceutical Ingredient

Flutamide API Manufacturer & Supplier in India

Also known as: Eulexin (brand)

CAS: 13311-84-7 Antiandrogen / Antineoplastic IP / BP / USP Bulk Supply Available
Flutamide API Manufacturer India | Mediocon Inc
Flutamide — Pharmaceutical Grade API

Product Overview

CAS No: 13311-84-7  |  MF: C₁₁H₁₁F₃N₂O₃  |  MW: 276.21 g/mol

Flutamide is a non-steroidal antiandrogen used primarily in the treatment of prostate cancer. It works by competitively blocking dihydrotestosterone (DHT) from binding to androgen receptors, thereby inhibiting tumor growth in hormone-sensitive prostate cancers.

Mediocon Inc supplies Flutamide IP/BP/USP as a certified active pharmaceutical ingredient for oncology pharmaceutical manufacturers globally. Manufactured under strict GMP conditions, our Flutamide meets full pharmacopoeial requirements with comprehensive analytical documentation.

Key Features

  • Non-steroidal androgen receptor antagonist
  • Competitive DHT blocker
  • GMP-certified production
  • Suitable for prostate cancer formulations

Applications

  • Prostate cancer (CRPC) therapy
  • Hormonal therapy combination regimens
  • Anti-androgen formulations
  • Oncology research & clinical 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 NameFlutamide
CAS Number13311-84-7
Molecular FormulaC₁₁H₁₁F₃N₂O₃
Molecular Weight276.21 g/mol
CategoryAntiandrogen / Antineoplastic
AppearancePale Yellow Crystalline Powder
GradeIP / BP / USP
Packaging25 kg HDPE Drums / Aluminium Bags
StorageCool, Dry & Ventilated Place

Analytical Specifications

ParameterSpecification
AssayNLT 98.5% & NMT 101.5%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 10 ppm
Residual SolventsComplies ICH Q3C
Microbial LimitsComplies
IdentificationHPLC & IR Compliant
Melting Point111 – 113 °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 Flutamide (CAS 13311-84-7) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Flutamide 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 — Flutamide API

What is the minimum order quantity for Flutamide API?
Mediocon Inc supplies Flutamide 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 Flutamide does Mediocon supply?
We supply Flutamide 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 Flutamide API?
Every shipment of Flutamide 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 Flutamide bulk orders?
Standard lead time for Flutamide 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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