Active Pharmaceutical Ingredient

Agomelatine API Manufacturer & Supplier in India

Also known as: Valdoxan

CAS: 138112-76-2 Antidepressant / CNS EP Standard Bulk Supply Available
Agomelatine API Manufacturer India | Mediocon Inc
Agomelatine — Pharmaceutical Grade API

Product Overview

CAS No: 138112-76-2  |  MF: C₁₅H₁₇NO₂  |  MW: 243.30 g/mol

Agomelatine is a novel antidepressant acting as a melatonin receptor agonist (MT1/MT2) and a serotonin receptor antagonist (5-HT2C). It resynchronizes circadian rhythms and improves sleep quality. Mediocon Inc supplies pharmaceutical-grade Agomelatine for licensed pharmaceutical manufacturers.

Key Features

  • Unique melatonergic antidepressant
  • EP compliant quality
  • Circadian rhythm resynchronization
  • Improved tolerability vs classical antidepressants

Applications

  • Major depressive disorder tablets
  • Circadian rhythm disorder treatment
  • Insomnia-associated depression
  • Specialty CNS formulations

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 NameAgomelatine
Also Known AsValdoxan
CAS Number138112-76-2
Molecular FormulaC₁₅H₁₇NO₂
Molecular Weight243.30 g/mol
CategoryAntidepressant / Melatonergic Agent
AppearanceWhite to Off-white Powder
GradeEP / In-house Standard

Analytical Specifications

ParameterSpecification
Assay98.0% – 102.0%
Loss on DryingNMT 0.5%
Melting Point95°C – 99°C
Heavy MetalsNMT 10 ppm
pHN/A
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Packing1 kg foil pouches / 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 Agomelatine (CAS 138112-76-2) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Agomelatine 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 — Agomelatine API

What is the minimum order quantity for Agomelatine API?
Mediocon Inc supplies Agomelatine 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 Agomelatine does Mediocon supply?
We supply Agomelatine conforming to EP / In-house Standard 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 Agomelatine API?
Every shipment of Agomelatine 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 Agomelatine bulk orders?
Standard lead time for Agomelatine 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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