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