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