Active Pharmaceutical Ingredient

Doramectin Manufacturer & Supplier in India

Also known as: Dectomax

CAS: 117704-25-3 Antiparasitic Agent (Avermectin, Veterinary) Pharma Grade GMP Certified Aurangabad, Maharashtra, India
Doramectin API — Mediocon Inc
Doramectin — Pharmaceutical Grade API

Product Overview

CAS No: 117704-25-3  |  MF: C50H74O14  |  MW: 899.10

Doramectin is a pharmaceutical-grade active ingredient classified as Antiparasitic Agent (Avermectin, Veterinary). Mediocon Inc supplies high-purity Doramectin API conforming to Pharma Grade specifications, manufactured in our GMP-certified facility in Aurangabad, Maharashtra, India.

Doramectin binds to glutamate-gated chloride channels in parasite nerve and muscle cells, causing paralysis and death of endo- and ecto-parasites. It is used as a critical raw material in finished dosage form manufacturing for global pharmaceutical markets.

Key Features

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

Applications

  • Veterinary endoparasite control
  • Ectoparasite (mite/tick) control
  • Livestock injectable antiparasitic formulations
  • Animal health pharmaceutical manufacturing

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 NameDoramectin
CAS Number117704-25-3
Molecular FormulaC50H74O14
Molecular Weight899.10
CategoryAntiparasitic Agent (Avermectin, Veterinary)
AppearanceWhite to off-white crystalline powder
GradePharma Grade
Batch NoMDCDOR2503310
Mfg DateMAR 2025
Exp DateFEB 2030
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 Doramectin (pharmaceutical grade) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Doramectin 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 — Doramectin API

What is the minimum order quantity for Doramectin API?
Mediocon Inc supplies Doramectin 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 Doramectin does Mediocon supply?
We supply Doramectin conforming to Pharma Grade 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 Doramectin API?
Every shipment of Doramectin 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 Doramectin bulk orders?
Standard lead time for Doramectin 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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