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