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