01 1LUPIN LIMITED.
01 1Tenofovir disoproxil fumarate
01 1India
Registration Number : 229MF10172
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2017-08-28
Latest Date of Registration : 2017-08-28
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PharmaCompass offers a list of Tenofovir Disoproxil Fumarate 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 Tenofovir Disoproxil Fumarate manufacturer or Tenofovir Disoproxil Fumarate supplier for your needs.
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PharmaCompass also assists you with knowing the Tenofovir Disoproxil Fumarate API Price utilized in the formulation of products. Tenofovir Disoproxil Fumarate API Price is not always fixed or binding as the Tenofovir Disoproxil Fumarate Price is obtained through a variety of data sources. The Tenofovir Disoproxil Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tenfovir disoproxil fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenfovir disoproxil fumarate, including repackagers and relabelers. The FDA regulates Tenfovir disoproxil fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenfovir disoproxil fumarate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tenfovir disoproxil fumarate supplier is an individual or a company that provides Tenfovir disoproxil fumarate active pharmaceutical ingredient (API) or Tenfovir disoproxil fumarate finished formulations upon request. The Tenfovir disoproxil fumarate suppliers may include Tenfovir disoproxil fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tenfovir disoproxil fumarate 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 Tenfovir disoproxil fumarate Drug Master File in Japan (Tenfovir disoproxil fumarate JDMF) empowers Tenfovir disoproxil fumarate 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 Tenfovir disoproxil fumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Tenfovir disoproxil fumarate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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