DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Changzhou Pharmaceutical Factory
03 1Hetero Labs Limited
01 3Lenalidomide
01 1China
02 2India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 306MF10010
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2024-01-17
Latest Date of Registration : 2024-01-17
Registration Number : 303MF10072
Registrant's Address : No. 518 Laodong East Road, Changzhou, Jiangsu, China
Initial Date of Registration : 2021-04-22
Latest Date of Registration : 2021-04-22
Registration Number : 304MF10029
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2022-02-10
Latest Date of Registration : 2022-02-10
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.
click here to find a list of Lenalidomide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Lenalidomide Drug Master File in Japan (Lenalidomide JDMF) empowers Lenalidomide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Lenalidomide JDMF during the approval evaluation for pharmaceutical products. At the time of Lenalidomide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Lenalidomide suppliers with JDMF on PharmaCompass.
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