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