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