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Fed Bioequivalence Study of Divalproex Sodium Delayed-Release Tablets, 500 mg

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01183676
Recruitment Status : Completed
First Posted : August 18, 2010
Last Update Posted : August 18, 2010
Information provided by:
Mylan Pharmaceuticals

No Study Results Posted on for this Study
  Recruitment Status : Completed
  Primary Completion Date : July 2007
  Study Completion Date : July 2007