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