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