Active Pharmaceutical Ingredient

Saxagliptin (CAS 47931-85-1) API Manufacturer & Supplier in India

Also known as: Saxagliptin Base; Onglyza

CAS: 47931-85-1 Antidiabetic / DPP-4 Inhibitor IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Saxagliptin API — Mediocon Inc, Aurangabad Maharashtra India
Saxagliptin — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 47931-85-1  |  MF: C₁₈H₂₅N₃O₂  |  MW: 315.41 g/mol

Saxagliptin is a potent, selective dipeptidyl peptidase-4 (DPP-4) inhibitor for the treatment of type 2 diabetes mellitus. Mediocon Inc supplies pharmaceutical-grade Saxagliptin conforming to IP / BP / EP / USP specifications from our GMP-certified facility in Aurangabad, Maharashtra, India.

Saxagliptin works by inhibiting the DPP-4 enzyme, prolonging the activity of incretin hormones (GLP-1 and GIP) that stimulate insulin secretion and suppress glucagon in a glucose-dependent manner.

Key Features

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

Applications

  • Type 2 diabetes mellitus treatment
  • DPP-4 inhibitor formulations
  • Glycaemic control medications
  • Combination antidiabetic tablets

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 NameSaxagliptin
Also Known AsSaxagliptin Base; Onglyza
CAS Number47931-85-1
Molecular FormulaC₁₈H₂₅N₃O₂
Molecular Weight315.41 g/mol
CategoryAntidiabetic / DPP-4 Inhibitor
AppearanceWhite to off-white crystalline powder
SolubilitySlightly soluble in water; 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
Mfg DateMAR 2025
Exp DateFEB 2030
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 Saxagliptin (CAS 47931-85-1) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Saxagliptin 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 — Saxagliptin API

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