Active Pharmaceutical Ingredient

Colistin API Manufacturer & Supplier in India

Also known as: Polymyxin E, Coly-Mycin (brand)

CAS: 1264-72-8 Polymyxin Antibiotic USP / BP / IP Bulk Supply Available
Colistin API Manufacturer India | Mediocon Inc
Colistin — Pharmaceutical Grade API

Product Overview

CAS No: 1264-72-8  |  MF: C₅₃H₁₀₀N₁₆O₁₃ (colistin A)  |  MW: 1168.46 g/mol

Colistin (Polymyxin E) is a last-resort antibiotic of the polymyxin class used for serious infections caused by multidrug-resistant (MDR) gram-negative bacteria including Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae. It disrupts bacterial outer membrane integrity. Mediocon Inc supplies pharmaceutical-grade Colistin Sulfate meeting IP/BP/EP/USP standards.

Key Features

  • Polymyxin class last-resort antibiotic
  • IP/BP/EP/USP compliant, Assay 99.0% Min.
  • Active against MDR Acinetobacter, Pseudomonas, Klebsiella
  • Suitable for IV, inhaled, and topical formulations

Applications

  • MDR Acinetobacter baumannii infections
  • Carbapenem-resistant Pseudomonas treatment
  • Klebsiella pneumoniae salvage therapy
  • Inhaled solution for lung infections in CF

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 NameColistin
Also Known AsPolymyxin E, Coly-Mycin (brand)
CAS Number1264-72-8
Molecular FormulaC₅₃H₁₀₀N₁₆O₁₃ (colistin A)
Molecular Weight1168.46 g/mol
CategoryAntibiotic / Polymyxin / Last-Resort
AppearanceWhite to Off-White Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay99.0% Min.
Loss on DryingNMT 5.0%
Heavy MetalsNMT 10 ppm
PotencyNot less than 19,000 IU/mg
Microbial LimitsComplies with pharmacopoeia
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 Colistin (CAS 1264-72-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Colistin 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 — Colistin API

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