Active Pharmaceutical Ingredient

Imipenem API Manufacturer & Supplier in India

Also known as: Primaxin (with Cilastatin)

CAS: 64221-86-9 Carbapenem Antibiotic IP / BP / EP / USP Bulk Supply Available
Imipenem API Manufacturer India | Mediocon Inc
Imipenem — Pharmaceutical Grade API

Product Overview

CAS No: 64221-86-9  |  MF: C₁₂H₁₇N₃O₄S  |  MW: 299.35 g/mol

Imipenem is a broad-spectrum carbapenem β-lactam antibiotic active against both gram-positive and gram-negative bacteria including Pseudomonas aeruginosa and Bacteroides fragilis. It is typically co-administered with cilastatin. Mediocon Inc supplies IP/BP/EP/USP compliant Imipenem API for injectable formulations.

Key Features

  • Ultra-broad spectrum carbapenem antibiotic
  • IP/BP/EP/USP compliant quality
  • Active against MDR gram-negative bacteria
  • For parenteral / injectable formulations

Applications

  • Serious polymicrobial infections
  • Hospital-acquired pneumonia (HAP)
  • Complicated intra-abdominal infections
  • MDR Pseudomonas aeruginosa infections

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 NameImipenem
Also Known AsPrimaxin (with Cilastatin)
CAS Number64221-86-9
Molecular FormulaC₁₂H₁₇N₃O₄S
Molecular Weight299.35 g/mol
CategoryCarbapenem Antibiotic
AppearanceWhite to Off-white Crystalline Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay97.0% – 102.0%
Loss on DryingNMT 1.5%
Heavy MetalsNMT 20 ppm
pH6.5 – 7.5 (1% solution)
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 Imipenem (CAS 64221-86-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Imipenem 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 — Imipenem API

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