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