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