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