A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Non-fasting Conditions
Status:
Completed
Trial end date:
2006-09-01
Target enrollment:
Participant gender:
Summary
To determine the pharmacokinetics and bioequivalence of cetirizine hydrochloride formulations
after administration of single doses to normal healthy subjects under fed conditions. These
data were to be evaluated statistically to determine if the products meet bioequivalence
criteria.