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