01 1Gilead Alberta ULC
02 1LUPIN LIMITED.
01 2Emtricitabine
01 1India
02 1U.S.A
Registration Number : 229MF10061
Registrant's Address : 1021 Hayter Road Edmonton, Alberta T6S 1A1, Canada
Initial Date of Registration : 2017-03-07
Latest Date of Registration : 2020-07-01
Registration Number : 229MF10167
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2017-08-22
Latest Date of Registration : 2017-08-22
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PharmaCompass offers a list of Emtricitabine 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 Emtricitabine manufacturer or Emtricitabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Emtricitabine manufacturer or Emtricitabine supplier.
PharmaCompass also assists you with knowing the Emtricitabine API Price utilized in the formulation of products. Emtricitabine API Price is not always fixed or binding as the Emtricitabine Price is obtained through a variety of data sources. The Emtricitabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TRUVADA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRUVADA, including repackagers and relabelers. The FDA regulates TRUVADA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRUVADA 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 TRUVADA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A TRUVADA supplier is an individual or a company that provides TRUVADA active pharmaceutical ingredient (API) or TRUVADA finished formulations upon request. The TRUVADA suppliers may include TRUVADA API manufacturers, exporters, distributors and traders.
click here to find a list of TRUVADA 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 TRUVADA Drug Master File in Japan (TRUVADA JDMF) empowers TRUVADA 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 TRUVADA JDMF during the approval evaluation for pharmaceutical products. At the time of TRUVADA 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 TRUVADA suppliers with JDMF on PharmaCompass.
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