Bioequivalence Study of Paroxetine Tablets and Paxil® Under Fasting and Fed Conditions in Chinese Healthy Volunteers
Status:
Completed
Trial end date:
2018-06-16
Target enrollment:
Participant gender:
Summary
The objective of this study is to compare the rate and extent of absorption of paroxetine
hydrochloride 20 mg tablets (test) and Paxil® (reference) administered as 20 mg tablet under
fed conditions.