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