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