Active Pharmaceutical Ingredient

Delavirdine API Manufacturer & Supplier in India

Also known as: Rescriptor

CAS: 136817-59-9 Antiretroviral / HIV Therapy USP / BP / IP / EP Bulk Supply Available
Delavirdine API Manufacturer India | Mediocon Inc
Delavirdine — Pharmaceutical Grade API

Product Overview

CAS No: 136817-59-9  |  MF: C₂₂H₂₈N₆O₃S  |  MW: 456.56 g/mol

Delavirdine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used in the treatment of HIV-1 infection in combination with other antiretroviral agents. It binds directly to reverse transcriptase and blocks RNA-dependent and DNA-dependent DNA polymerase activities. Mediocon Inc supplies pharmaceutical-grade Delavirdine meeting IP, BP, EP, and USP standards.

Key Features

  • Analgesic, antipyretic & anti-inflammatory
  • USP/BP/IP compliant quality
  • Widely used in cardiovascular therapy
  • Suitable for tablet and effervescent formulations

Applications

  • HIV-1 infection combination therapy
  • HAART (Highly Active Antiretroviral Therapy)
  • Antiretroviral drug formulations
  • HIV clinical research applications

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 NameDelavirdine
Also Known AsRescriptor
CAS Number136817-59-9
Molecular FormulaC₂₂H₂₈N₆O₃S
Molecular Weight456.56 g/mol
CategoryNon-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) / Antiretroviral
AppearanceWhite to Off-White Powder
GradeUSP / BP / IP / EP

Analytical Specifications

ParameterSpecification
Assay99.0% Min.
Loss on DryingNMT 0.5%
Melting PointN/A
Heavy MetalsNMT 20 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 Delavirdine (CAS 136817-59-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Delavirdine 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 — Delavirdine API

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