Pharmacokinetics: The effective concentration of Rebamipide is in the range of 1-1000 μm. The following table briefly explains the pharmacokinetic parameter of Rebamipide. (See table.)

Up to 98.4% of ingested Rebamipide is bound to plasma proteins. It is metabolized in the liver by human cytochrome P450 enzyme. The cytochrome P450 enzyme acts on Rebamipide through hydroxylation and glucuronidation, resulting in the formation of 6-hydroxy and 8-hydroxyrebamipide. The role of glucuronidation in the metabolism of rebamipide is very low and nonsignificant. Drug interactions of Rebamipide with other drugs is very low and safely used concomitantly with other drugs.