Active Pharmaceutical Ingredient

Bendamustine API Manufacturer & Supplier in India

Also known as: Treanda, Levact (brand)

CAS: 16506-27-7 Alkylating Agent USP / BP / IP Bulk Supply Available
Bendamustine API Manufacturer India | Mediocon Inc
Bendamustine — Pharmaceutical Grade API

Product Overview

CAS No: 16506-27-7  |  MF: C₁₆H₂₁ClN₄O₂  |  MW: 358.82 g/mol

Bendamustine is a bifunctional alkylating agent used for the treatment of chronic lymphocytic leukemia (CLL), non-Hodgkin lymphoma (NHL), and multiple myeloma. It combines the alkylating properties of nitrogen mustard with a purine-like benzimidazole ring. Mediocon Inc supplies pharmaceutical-grade Bendamustine meeting IP/BP/EP/USP standards.

Key Features

  • Bifunctional alkylating agent
  • IP/BP/EP/USP compliant quality
  • Treatment for CLL, NHL, and multiple myeloma
  • Suitable for IV infusion formulations

Applications

  • Chronic lymphocytic leukemia
  • Non-Hodgkin lymphoma treatment
  • Multiple myeloma therapy
  • Oncology IV formulations

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 NameBendamustine
Also Known AsTreanda, Levact (brand)
CAS Number16506-27-7
Molecular FormulaC₁₆H₂₁ClN₄O₂
Molecular Weight358.82 g/mol
CategoryOncology / Alkylating Agent
AppearanceWhite to Off-White Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay98.0% – 102.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
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 Bendamustine (CAS 16506-27-7) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Bendamustine 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 — Bendamustine API

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