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