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