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The principal cytochrome P450 isoenzyme included seems to get CYP2E1, with CYP1A2 and CYP3A4 as extra pathways. Somewhere around eighty five% of the oral dose seems while in the urine within just 24 hours of administration, most as being the glucuronide conjugate, with small quantities of other conjugates and unchanged drug (see OVERDOSAGE) for tox