Active Pharmaceutical Ingredient

Bexarotene API Manufacturer & Supplier in India

Also known as: Targretin (brand)

CAS: 153559-49-0 Retinoid / RXR Agonist USP / BP / IP Bulk Supply Available
Bexarotene API Manufacturer India | Mediocon Inc
Bexarotene — Pharmaceutical Grade API

Product Overview

CAS No: 153559-49-0  |  MF: C₂₄H₂₈O₂  |  MW: 348.48 g/mol

Bexarotene is a retinoid that selectively activates retinoid X receptors (RXRs). It is used for the treatment of cutaneous T-cell lymphoma (CTCL). Bexarotene induces differentiation and apoptosis in tumor cells. Mediocon Inc supplies pharmaceutical-grade Bexarotene meeting IP/BP/EP/USP standards.

Key Features

  • Selective RXR retinoid agonist
  • IP/BP/EP/USP compliant quality
  • Cutaneous T-cell lymphoma treatment
  • Available in oral and topical formulations

Applications

  • Oral capsules for CTCL
  • Topical gel formulations
  • Dermatological oncology
  • Pharmaceutical 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 NameBexarotene
Also Known AsTargretin (brand)
CAS Number153559-49-0
Molecular FormulaC₂₄H₂₈O₂
Molecular Weight348.48 g/mol
CategoryOncology / Retinoid / RXR Agonist
AppearanceWhite to Off-White Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay98.0% – 102.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
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 Bexarotene (CAS 153559-49-0) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Bexarotene 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 — Bexarotene API

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