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