A PHENYTOIN (5,5-DIPHENYLHYDANTOIN) DMF (Drug Master File) is a document detailing the whole manufacturing process of PHENYTOIN (5,5-DIPHENYLHYDANTOIN) active pharmaceutical ingredient (API) in detail. Different forms of PHENYTOIN (5,5-DIPHENYLHYDANTOIN) DMFs exist exist since differing nations have different regulations, such as PHENYTOIN (5,5-DIPHENYLHYDANTOIN) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A PHENYTOIN (5,5-DIPHENYLHYDANTOIN) DMF submitted to regulatory agencies in the US is known as a USDMF. PHENYTOIN (5,5-DIPHENYLHYDANTOIN) USDMF includes data on PHENYTOIN (5,5-DIPHENYLHYDANTOIN)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The PHENYTOIN (5,5-DIPHENYLHYDANTOIN) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of PHENYTOIN (5,5-DIPHENYLHYDANTOIN) suppliers with USDMF on PharmaCompass.