Active Pharmaceutical Ingredient

Ractopamine API Manufacturer & Supplier in India

Also known as: Paylean; Optaflexx; RU 28362

GMP Certified IP / BP / EP / USP β-Adrenergic Agonist Aurangabad, India
Ractopamine API Supplier Manufacturer Aurangabad Maharashtra India — Mediocon Inc
Ractopamine IP / BP / EP / USP  |  GMP Certified  |  Mediocon Inc, Maharashtra, India
CAS No: 97825-25-7

Product Overview

Ractopamine is a beta-adrenergic agonist that acts on β1 and β2 adrenergic receptors. It has been studied for its cardiac stimulant properties and is used in research and veterinary applications. Mediocon Inc manufactures GMP-compliant Ractopamine at its Aurangabad facility.

Therapeutic Applications
  • Beta-adrenergic receptor agonist
  • Cardiac stimulant
  • Repartitioning agent (veterinary and research)
  • Sympathomimetic applications

Technical Specifications

ParameterSpecification
CAS Number97825-25-7
Molecular FormulaC₁₈H₂₃NO₃
Molecular Weight301.38 g/mol
GradeIP / BP / EP / USP
Categoryβ-Adrenergic Agonist
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Batch NoRAC/24032026
Mfg DateMAR 2026
Exp DateFEB 2031
Packing25 kg HDPE drums / as per requirement

Quality & Compliance

  • GMP Certified manufacturing facility in Aurangabad, Maharashtra, India
  • Full pharmacopoeial compliance: IP / BP / EP / USP standards
  • Complete documentation: Certificate of Analysis (CoA), MSDS, Certificate of Origin
  • Stringent in-process quality control at every manufacturing stage
  • HPLC purity testing and spectroscopic identification (IR, NMR)
  • Cold-chain and controlled-environment storage facilities available
  • Exported to 40+ countries with full regulatory support

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 Ractopamine — CAS 97825-25-7 (CAS 97825-25-7) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Ractopamine — CAS 97825-25-7 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 — Ractopamine — CAS 97825-25-7 API

What is the minimum order quantity for Ractopamine — CAS 97825-25-7 API?
Mediocon Inc supplies Ractopamine — CAS 97825-25-7 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 Ractopamine — CAS 97825-25-7 does Mediocon supply?
We supply Ractopamine — CAS 97825-25-7 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 Ractopamine — CAS 97825-25-7 API?
Every shipment of Ractopamine — CAS 97825-25-7 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 Ractopamine — CAS 97825-25-7 bulk orders?
Standard lead time for Ractopamine — CAS 97825-25-7 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.

Request a Quote

Minimum Order: 1 kg (sample available)
Export to 40+ countries worldwide
Full documentation: CoA, MSDS, COO
Lead Time: 2–4 weeks (standard)
WhatsApp: +91 9309999757
akshay@mediocon.com
 Get Bulk Quote  Request CoA / MSDS

Quick Reference

CAS No97825-25-7
FormulaC₁₈H₂₃NO₃
MW301.38 g/mol
GradeIP / BP / EP / USP
Categoryβ-Adrenergic Agonist

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