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