Active Pharmaceutical Ingredient

Rilpivirine API Manufacturer & Supplier in India

Also known as: Edurant; TMC278; R278474

GMP Certified IP / BP / EP / USP Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) / Antiretroviral Aurangabad, India
Rilpivirine API Supplier Manufacturer Aurangabad Maharashtra India — Mediocon Inc
Rilpivirine IP / BP / EP / USP  |  GMP Certified  |  Mediocon Inc, Maharashtra, India
CAS No: 132907-72-3

Product Overview

Rilpivirine is a high-purity Active Pharmaceutical Ingredient (API) classified as a Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) for HIV treatment. Mediocon Inc manufactures GMP-compliant Rilpivirine at its facility in Aurangabad, Maharashtra, India.

Therapeutic Applications
  • HIV-1 infection treatment in combination ART regimens
  • Treatment-naive HIV-1 infected adults
  • Single-tablet regimen components
  • Long-acting injectable antiretroviral formulations

Technical Specifications

ParameterSpecification
CAS Number132907-72-3
Molecular FormulaC₂₂H₁₈N₆
Molecular Weight366.42 g/mol
GradeIP / BP / EP / USP
CategoryNon-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) / Antiretroviral
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 NoRLP/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 Rilpivirine — CAS 132907-72-3 (CAS 132907-72-3) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Rilpivirine — CAS 132907-72-3 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 — Rilpivirine — CAS 132907-72-3 API

What is the minimum order quantity for Rilpivirine — CAS 132907-72-3 API?
Mediocon Inc supplies Rilpivirine — CAS 132907-72-3 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 Rilpivirine — CAS 132907-72-3 does Mediocon supply?
We supply Rilpivirine — CAS 132907-72-3 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 Rilpivirine — CAS 132907-72-3 API?
Every shipment of Rilpivirine — CAS 132907-72-3 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 Rilpivirine — CAS 132907-72-3 bulk orders?
Standard lead time for Rilpivirine — CAS 132907-72-3 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 No132907-72-3
FormulaC₂₂H₁₈N₆
MW366.42 g/mol
GradeIP / BP / EP / USP
CategoryNon-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) / Antiretroviral

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