Active Pharmaceutical Ingredient

Ergotamine Tartrate API Manufacturer & Supplier in India

High-purity Ergotamine Tartrate API — GMP Certified

CAS: 379-79-3 IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Ergotamine Tartrate API Manufacturer In India — Mediocon Inc
Ergotamine Tartrate API Manufacturer In India — Pharmaceutical Grade API

Product Overview

CAS No: 379-79-3  |  MF: C33H35N5O5·C4H6O6  |  MW: 656.71

Ergotamine Tartrate is an ergot alkaloid used as an antimigraine agent for the treatment of acute migraine and cluster headaches. Mediocon Inc manufactures Ergotamine Tartrate API to IP/BP/EP/USP pharmacopoeial standards in its GMP-certified facility in Aurangabad, Maharashtra, India.

Our Ergotamine Tartrate API is supplied to pharmaceutical manufacturers of antimigraine tablets, sublingual tablets, and suppositories globally with full quality documentation and regulatory support.

Key Features

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

Applications

  • Acute migraine treatment formulations
  • Cluster headache therapy
  • Antimigraine tablet and suppository manufacturing
  • Vascular headache management

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 NameErgotamine Tartrate
CAS Number379-79-3
Molecular FormulaC33H35N5O5·C4H6O6
Molecular Weight656.71
CategoryActive Pharmaceutical Ingredient
AppearanceWhite to off-white crystalline powder
GradeIP / BP / EP / USP
Batch NoPEMD/24032026
Mfg DateMAR 2026
Exp DateFEB 2031
Quantity25.00 Kg
Gross Weight26.00 Kg

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 Ergotamine Tartrate (CAS 379-79-3) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Ergotamine Tartrate 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 — Ergotamine Tartrate API

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