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