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