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