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