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