Active Pharmaceutical Ingredient

Delamanid (CAS 681492-22-8) API Manufacturer & Supplier in India

Also known as: Deltyba / OPC-67683

CAS: 681492-22-8 Anti-TB / Antibacterial USP / BP / IP / EP Bulk Supply Available
Delamanid API Manufacturer India | Mediocon Inc
Delamanid — Pharmaceutical Grade API

Product Overview

CAS No: 681492-22-8  |  MF: C₂₅H₂₅F₃N₄O₆  |  MW: 534.48 g/mol

Delamanid is a nitroimidazole-oxazole compound used for the treatment of multidrug-resistant tuberculosis (MDR-TB) as part of an appropriate combination regimen. It inhibits mycolic acid synthesis, disrupting the bacterial cell wall of Mycobacterium tuberculosis. Mediocon Inc supplies pharmaceutical-grade Delamanid 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

  • Multidrug-resistant tuberculosis (MDR-TB)
  • Extensively drug-resistant TB (XDR-TB)
  • Combination anti-TB regimens
  • TB R&D and clinical research

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 NameDelamanid
Also Known AsDeltyba / OPC-67683
CAS Number681492-22-8
Molecular FormulaC₂₅H₂₅F₃N₄O₆
Molecular Weight534.48 g/mol
CategoryNitroimidazole Antibiotic / Anti-tuberculosis Agent
AppearanceWhite to Pale Yellow 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 Delamanid (CAS 681492-22-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Delamanid 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 — Delamanid API

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