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