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