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PharmaCompass offers a list of Fenofibrate 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 Fenofibrate manufacturer or Fenofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fenofibrate manufacturer or Fenofibrate supplier.
PharmaCompass also assists you with knowing the Fenofibrate API Price utilized in the formulation of products. Fenofibrate API Price is not always fixed or binding as the Fenofibrate Price is obtained through a variety of data sources. The Fenofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenofibrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenofibrate, including repackagers and relabelers. The FDA regulates Fenofibrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenofibrate 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 Fenofibrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenofibrate supplier is an individual or a company that provides Fenofibrate active pharmaceutical ingredient (API) or Fenofibrate finished formulations upon request. The Fenofibrate suppliers may include Fenofibrate API manufacturers, exporters, distributors and traders.
click here to find a list of Fenofibrate 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 Fenofibrate Drug Master File in Korea (Fenofibrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fenofibrate. The MFDS reviews the Fenofibrate KDMF as part of the drug registration process and uses the information provided in the Fenofibrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fenofibrate 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 Fenofibrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fenofibrate suppliers with KDMF on PharmaCompass.
We have 9 companies offering Fenofibrate
Get in contact with the supplier of your choice: