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