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