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