Active Pharmaceutical Ingredient

Inamrinone API Manufacturer & Supplier in India

Also known as: Amrinone / Inocor

CAS: 60719-84-8 Phosphodiesterase Inhibitor / Cardiotonic IP / BP / EP / USP Bulk Supply Available
Inamrinone API Manufacturer India | Mediocon Inc
Inamrinone — Pharmaceutical Grade API

Product Overview

CAS No: 60719-84-8  |  MF: C₁₀H₉N₃O  |  MW: 187.20 g/mol

Inamrinone (formerly Amrinone) is a phosphodiesterase III inhibitor with positive inotropic and vasodilatory properties used in the short-term management of decompensated heart failure. Mediocon Inc supplies IP/BP/EP/USP compliant Inamrinone API for injectable formulations.

Key Features

  • PDE-III inhibitor with inotropic activity
  • IP/BP/EP/USP compliant quality
  • Suitable for parenteral formulations
  • For acute heart failure management

Applications

  • Short-term management of decompensated heart failure
  • Inotropic support in ICU settings
  • Perioperative cardiac support
  • Acute hemodynamic stabilization

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 NameInamrinone
Also Known AsAmrinone / Inocor
CAS Number60719-84-8
Molecular FormulaC₁₀H₉N₃O
Molecular Weight187.20 g/mol
CategoryPhosphodiesterase Inhibitor / Cardiotonic
AppearanceYellow Crystalline Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay98.0% – 102.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
pH3.2 – 4.0 (parenteral 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 Inamrinone (CAS 60719-84-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Inamrinone 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 — Inamrinone API

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