A Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) DMF (Drug Master File) is a document detailing the whole manufacturing process of Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) active pharmaceutical ingredient (API) in detail. Different forms of Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) DMFs exist exist since differing nations have different regulations, such as Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) DMF submitted to regulatory agencies in the US is known as a USDMF. Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) USDMF includes data on Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Guanidine, [(3-iodophenyl)methyl]-, sulfate (2:1) USDMF is kept confidential to protect the manufacturer’s intellectual property.
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