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