01 1HETERO DRUGS LIMITED.
01 1Ritonavir
01 1India
Registration Number : 306MF10153
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
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, Price,and more, enabling you to easily find the right Ritonavir manufacturer or Ritonavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ritonavir manufacturer or Ritonavir supplier.
PharmaCompass also assists you with knowing the Ritonavir API Price utilized in the formulation of products. Ritonavir API Price is not always fixed or binding as the Ritonavir Price is obtained through a variety of data sources. The Ritonavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RIT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RIT, including repackagers and relabelers. The FDA regulates RIT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RIT 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 RIT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RIT supplier is an individual or a company that provides RIT active pharmaceutical ingredient (API) or RIT finished formulations upon request. The RIT suppliers may include RIT API manufacturers, exporters, distributors and traders.
click here to find a list of RIT 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 RIT Drug Master File in Japan (RIT JDMF) empowers RIT 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 RIT JDMF during the approval evaluation for pharmaceutical products. At the time of RIT 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 RIT suppliers with JDMF on PharmaCompass.
