Bioequivalence Study of Divalproex Sodium DR Tablets 500 mg of Dr. Reddy's Under Fed Conditions
Status:
Completed
Trial end date:
2006-11-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to assess the bioavailability of Divalproex Sodium DR Tablets
500 mg versus Depakote DR 500 mg tablets with a washout period of 10 days in healthy
subjects.