A Fenytoine DMF (Drug Master File) is a document detailing the whole manufacturing process of Fenytoine active pharmaceutical ingredient (API) in detail. Different forms of Fenytoine DMFs exist exist since differing nations have different regulations, such as Fenytoine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fenytoine DMF submitted to regulatory agencies in the US is known as a USDMF. Fenytoine USDMF includes data on Fenytoine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fenytoine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fenytoine suppliers with USDMF on PharmaCompass.