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