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