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