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