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