01 1HETERO DRUGS LIMITED.
01 1Ritonavir
01 1India
Registration Number : 306MF10153
Registrant's Address : 7-2-A2, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telangana, INDIA
Initial Date of Registration : 2024-11-27
Latest Date of Registration : 2025-03-19
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PharmaCompass offers a list of Ritonavir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ritonavir manufacturer or Ritonavir supplier for your needs.
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A 3prs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3prs, including repackagers and relabelers. The FDA regulates 3prs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3prs 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 3prs manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 3prs supplier is an individual or a company that provides 3prs active pharmaceutical ingredient (API) or 3prs finished formulations upon request. The 3prs suppliers may include 3prs API manufacturers, exporters, distributors and traders.
click here to find a list of 3prs suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 3prs Drug Master File in Japan (3prs JDMF) empowers 3prs 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 3prs JDMF during the approval evaluation for pharmaceutical products. At the time of 3prs 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 3prs suppliers with JDMF on PharmaCompass.
