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