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