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