Active Pharmaceutical Ingredient

Bimatoprost API Manufacturer & Supplier in India

Also known as: Bimatoprost Ophthalmic; Lumigan API

CAS: 155206-00-1 Antiglaucoma IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Bimatoprost API — Mediocon Inc
Bimatoprost — Pharmaceutical Grade API

Product Overview

CAS No: 155206-00-1  |  MF: C₂₅H₃₇NO₄  |  MW: 415.57 g/mol

Bimatoprost is a synthetic prostamide analogue used as an active pharmaceutical ingredient in ophthalmic solutions. Mediocon Inc supplies high-purity Bimatoprost API conforming to IP / BP / EP / USP specifications from our GMP-certified facility in Aurangabad, Maharashtra, India.

Bimatoprost lowers intraocular pressure (IOP) by mimicking the effects of naturally occurring prostamides. It is used in the treatment of open-angle glaucoma and ocular hypertension and is also indicated for hypotrichosis of the eyelashes.

Key Features

  • High-purity pharmaceutical grade API
  • IP / BP / EP / USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing

Applications

  • Open-angle glaucoma treatment
  • Ocular hypertension management
  • Eyelash growth formulations (hypotrichosis)
  • Ophthalmic prostaglandin formulations

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 NameBimatoprost
Also Known AsBimatoprost Ophthalmic; Lumigan API
CAS Number155206-00-1
Molecular FormulaC₂₅H₃₇NO₄
Molecular Weight415.57 g/mol
CategoryProstaglandin Analogue — Antiglaucoma
AppearanceWhite to off-white crystalline powder
SolubilitySlightly soluble in water; soluble in ethanol
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
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 Bimatoprost (CAS 155206-00-1) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Bimatoprost 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 — Bimatoprost API

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