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