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