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