Bioequivalence Study of Sertraline Hydrochloride 100mg Tablets Under Fed Conditions
Status:
Completed
Trial end date:
2005-10-01
Target enrollment:
Participant gender:
Summary
The purpose of this study was to evaluate the relative bioavailability of the test
formulation of sertraline 100 mg tablets with an already marketed reference formulation
Zoloft® 100 mg tablets (Pfizer), under non-fasting conditions in healthy male and female
adult subjects.