Active Pharmaceutical Ingredient

Amiodarone API Manufacturer & Supplier in India

Also known as: Cordarone

CAS: 1951-25-3 Antiarrhythmic / Cardiology USP / BP / IP Bulk Supply Available
Amiodarone API Manufacturer India | Mediocon Inc
Amiodarone — Pharmaceutical Grade API

Product Overview

CAS No: 1951-25-3  |  MF: C₂₅H₂₉I₂NO₃  |  MW: 645.31 g/mol

Amiodarone hydrochloride is a class III antiarrhythmic agent used to treat ventricular and supraventricular arrhythmias. It prolongs the cardiac action potential by blocking potassium channels. Mediocon Inc supplies pharmaceutical-grade Amiodarone meeting USP, BP, and IP standards.

Key Features

  • Class III antiarrhythmic (potassium channel blocker)
  • USP/BP/IP compliant quality
  • Effective for both ventricular & supraventricular arrhythmias
  • Suitable for oral and IV formulations

Applications

  • Ventricular tachycardia/fibrillation tablets
  • Atrial fibrillation & flutter
  • IV injectable for acute arrhythmias
  • Post-cardiac surgery prophylaxis

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 NameAmiodarone
Also Known AsCordarone
CAS Number1951-25-3
Molecular FormulaC₂₅H₂₉I₂NO₃
Molecular Weight645.31 g/mol
CategoryClass III Antiarrhythmic
AppearanceWhite to Off-white Powder
GradeUSP / BP / IP

Analytical Specifications

ParameterSpecification
Assay98.0% – 101.0%
Loss on DryingNMT 0.5%
Melting Point158°C – 162°C
Heavy MetalsNMT 10 ppm
pH3.0 – 4.0 (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 Amiodarone (CAS 1951-25-3) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Amiodarone 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 — Amiodarone API

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