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Clamoxyl is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Clamoxyl and M1 occurs at two and three hours, respectively, after administration in healthy adults.