Active Pharmaceutical Ingredient

Amisulpride API Manufacturer & Supplier in India

Also known as: Solian

CAS: 71675-85-9 Antipsychotic / CNS BP / EP Bulk Supply Available
Amisulpride API Manufacturer India | Mediocon Inc
Amisulpride — Pharmaceutical Grade API

Product Overview

CAS No: 71675-85-9  |  MF: C₁₇H₂₇N₃O₄S  |  MW: 369.48 g/mol

Amisulpride is an atypical antipsychotic of the benzamide class that selectively blocks dopamine D2 and D3 receptors. At low doses it acts as a presynaptic blocker improving negative symptoms; at higher doses it treats positive symptoms of schizophrenia. Mediocon Inc supplies pharmaceutical-grade Amisulpride meeting BP and EP standards.

Key Features

  • Selective D2/D3 receptor antagonist
  • BP/EP compliant quality
  • Effective for both positive & negative symptoms
  • Suitable for tablet formulations

Applications

  • Schizophrenia tablets
  • Dysthymia and negative symptom treatment
  • Acute psychosis management
  • Maintenance antipsychotic therapy

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 NameAmisulpride
Also Known AsSolian
CAS Number71675-85-9
Molecular FormulaC₁₇H₂₇N₃O₄S
Molecular Weight369.48 g/mol
CategoryAtypical Antipsychotic / Benzamide
AppearanceWhite to Off-white Crystalline Powder
GradeBP / EP

Analytical Specifications

ParameterSpecification
Assay99.0% – 101.0%
Loss on DryingNMT 0.5%
Melting Point124°C – 128°C
Heavy MetalsNMT 10 ppm
pHN/A
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 Amisulpride (CAS 71675-85-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Amisulpride 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 — Amisulpride API

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