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