DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
01 1Pomalidomide
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 307MF10051
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2025-04-08
Latest Date of Registration : 2025-04-08
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PharmaCompass offers a list of Pomalidomide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pomalidomide manufacturer or Pomalidomide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pomalidomide manufacturer or Pomalidomide supplier.
PharmaCompass also assists you with knowing the Pomalidomide API Price utilized in the formulation of products. Pomalidomide API Price is not always fixed or binding as the Pomalidomide Price is obtained through a variety of data sources. The Pomalidomide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IMiD1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IMiD1, including repackagers and relabelers. The FDA regulates IMiD1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IMiD1 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 IMiD1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A IMiD1 supplier is an individual or a company that provides IMiD1 active pharmaceutical ingredient (API) or IMiD1 finished formulations upon request. The IMiD1 suppliers may include IMiD1 API manufacturers, exporters, distributors and traders.
click here to find a list of IMiD1 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 IMiD1 Drug Master File in Japan (IMiD1 JDMF) empowers IMiD1 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 IMiD1 JDMF during the approval evaluation for pharmaceutical products. At the time of IMiD1 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 IMiD1 suppliers with JDMF on PharmaCompass.
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