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