DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddy's Laboratories
02 1M/s Alembic Pharmaceuticals Limited
03 1M/s Biocon Limited
04 1M/s Shilpa Medicare Limited
05 1M/s. Alembic Pharmaceuticals Limited
06 1M/s. Cipla Limited
07 1M/s. Hetro Labs Limited
08 1M/s. Laurus Labs Pvt. Ltd
09 1M/s. Laurus Labs Pvt. Ltd.,
10 1M/s. Mylan Lab Ltd.
11 1M/s. Reliance Life Sciences Pvt. Ltd.
12 1M/s. Sun Pharmaceuticals Industries Ltd.
13 1MSN Laboratories Pvt. Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
A Lenalidomide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lenalidomide, including repackagers and relabelers. The FDA regulates Lenalidomide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lenalidomide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lenalidomide supplier is an individual or a company that provides Lenalidomide active pharmaceutical ingredient (API) or Lenalidomide finished formulations upon request. The Lenalidomide suppliers may include Lenalidomide API manufacturers, exporters, distributors and traders.
click here to find a list of Lenalidomide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lenalidomide written confirmation (Lenalidomide WC) is an official document issued by a regulatory agency to a Lenalidomide manufacturer, verifying that the manufacturing facility of a Lenalidomide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lenalidomide APIs or Lenalidomide finished pharmaceutical products to another nation, regulatory agencies frequently require a Lenalidomide WC (written confirmation) as part of the regulatory process.
click here to find a list of Lenalidomide suppliers with Written Confirmation (WC) on PharmaCompass.
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