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