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