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