Bioequivalence Study of Levocetirizine Dihydrochloride Tablets 5 mg Under Fasting Condition
Status:
Completed
Trial end date:
2012-03-01
Target enrollment:
Participant gender:
Summary
This is a single-dose, Randomized, two-period,cross over pivotal study. The purpose of this
study is to assess the bioequivalence between Test Product and the corresponding Reference
Product under fasting condition in normal, healthy, adult, human subjects.