01 1LUPIN LIMITED.
02 1PharmaChem Technologies G. B. Ltd.
01 1Tenofovir Disoproxil Fumarate
02 1Tenofovir disoproxil fumarate
01 1Bahamas
02 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
Registration Number : 225MF10169
Registrant's Address : West Sunrise Highway P. O. Box F-42430 Freeport, Grand Bahamas
Initial Date of Registration : 2013-08-28
Latest Date of Registration : 2017-10-03
A Tenofovir Disoproxil Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Disoproxil Fumarate, including repackagers and relabelers. The FDA regulates Tenofovir Disoproxil Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir 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.
click here to find a list of Tenofovir Disoproxil Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenofovir Disoproxil Fumarate supplier is an individual or a company that provides Tenofovir Disoproxil Fumarate active pharmaceutical ingredient (API) or Tenofovir Disoproxil Fumarate finished formulations upon request. The Tenofovir Disoproxil Fumarate suppliers may include Tenofovir Disoproxil Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tenofovir 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 Tenofovir Disoproxil Fumarate Drug Master File in Japan (Tenofovir Disoproxil Fumarate JDMF) empowers Tenofovir 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 Tenofovir Disoproxil Fumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Tenofovir 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.
click here to find a list of Tenofovir Disoproxil Fumarate suppliers with JDMF on PharmaCompass.
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