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