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PharmaCompass offers a list of Entecavir 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 Entecavir manufacturer or Entecavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Entecavir manufacturer or Entecavir supplier.
PharmaCompass also assists you with knowing the Entecavir API Price utilized in the formulation of products. Entecavir API Price is not always fixed or binding as the Entecavir Price is obtained through a variety of data sources. The Entecavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CID153941 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CID153941, including repackagers and relabelers. The FDA regulates CID153941 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CID153941 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 CID153941 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CID153941 supplier is an individual or a company that provides CID153941 active pharmaceutical ingredient (API) or CID153941 finished formulations upon request. The CID153941 suppliers may include CID153941 API manufacturers, exporters, distributors and traders.
click here to find a list of CID153941 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 CID153941 Drug Master File in Korea (CID153941 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CID153941. The MFDS reviews the CID153941 KDMF as part of the drug registration process and uses the information provided in the CID153941 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CID153941 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 CID153941 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CID153941 suppliers with KDMF on PharmaCompass.
We have 14 companies offering CID153941
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