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