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 Revlimid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Revlimid, including repackagers and relabelers. The FDA regulates Revlimid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Revlimid 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 Revlimid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Revlimid supplier is an individual or a company that provides Revlimid active pharmaceutical ingredient (API) or Revlimid finished formulations upon request. The Revlimid suppliers may include Revlimid API manufacturers, exporters, distributors and traders.
click here to find a list of Revlimid 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 Revlimid Drug Master File in Japan (Revlimid JDMF) empowers Revlimid 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 Revlimid JDMF during the approval evaluation for pharmaceutical products. At the time of Revlimid 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 Revlimid suppliers with JDMF on PharmaCompass.
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