A n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea DMF (Drug Master File) is a document detailing the whole manufacturing process of n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea active pharmaceutical ingredient (API) in detail. Different forms of n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea DMFs exist exist since differing nations have different regulations, such as n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea DMF submitted to regulatory agencies in the US is known as a USDMF. n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea USDMF includes data on n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The n-(1-Adamantyl)-n'-(4-guanidinobenzyl)urea USDMF is kept confidential to protect the manufacturer’s intellectual property.
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