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