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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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a TRUVADA Drug Master File in Korea (TRUVADA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of TRUVADA. The MFDS reviews the TRUVADA KDMF as part of the drug registration process and uses the information provided in the TRUVADA KDMF to evaluate the safety and efficacy of the drug.
After submitting a TRUVADA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their TRUVADA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of TRUVADA suppliers with KDMF on PharmaCompass.
We have 5 companies offering TRUVADA
Get in contact with the supplier of your choice: