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