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