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A Relative Bioavailability Study of Propranolol HCl 160 mg Tablets Under Non-fasting Conditions

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.
ClinicalTrials.gov Identifier: NCT00864747
Recruitment Status : Completed
First Posted : March 19, 2009
Last Update Posted : August 17, 2010
Sponsor:
Information provided by:
Actavis Inc.

No Study Results Posted on ClinicalTrials.gov for this Study
  Recruitment Status : Completed
  Primary Completion Date : May 2005
  Study Completion Date : May 2005