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