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