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