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