Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting

Bioequivalence Study of Divalproex Sodium ER Tablets, 500 mg Under Fed Conditions

This study has been completed.
Information provided by (Responsible Party):
Dr. Reddy's Laboratories Limited Identifier:
First received: April 4, 2012
Last updated: April 19, 2012
Last verified: April 2012
No Study Results Posted on for this Study
  Study Status: This study has been completed.
  Study Completion Date: March 2011
  Primary Completion Date: February 2011 (Final data collection date for primary outcome measure)