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