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