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