Active Pharmaceutical Ingredient

Nateglinide API Manufacturer & Supplier in India

Also known as: Starlix; Fastic

CAS: 105816-04-4 Meglitinide Antidiabetic IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Nateglinide API — Mediocon Inc
Nateglinide — Pharmaceutical Grade API

Product Overview

CAS No: 105816-04-4  |  MF: C₁₉H₂₇NO₃  |  MW: 317.42 g/mol

Mirtazapine is a pharmaceutical-grade active ingredient classified as Meglitinide Antidiabetic. Mediocon Inc supplies high-purity Nateglinide conforming to IP / BP / EP / USP specifications, manufactured in our GMP-certified facility in Aurangabad, Maharashtra, India.

Key Features

  • Rapid-acting insulin secretagogue
  • IP/BP/EP/USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing

Applications

  • Type 2 diabetes mellitus
  • Post-meal glucose control
  • Combination therapy with metformin

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 NameNateglinide
Also Known AsStarlix; Fastic
CAS Number105816-04-4
Chemical NameN-[(trans-4-isopropylcyclohexyl)carbonyl]-D-phenylalanine
Molecular FormulaC₁₉H₂₇NO₃
Molecular Weight317.42 g/mol
CategoryNaSSA Antidepressant
AppearanceWhite to off-white powder
SolubilityPractically insoluble in water at neutral pH; soluble in methanol
GradeIP / BP / EP / USP

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 Nateglinide (CAS 105816-04-4) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Nateglinide 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 — Nateglinide API

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