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

Fasting Bioequivalence Study of Pravastatin Sodium 80 mg Tablets Versus Pravachol® 80 mg Tablets In Normal Healthy Subjects

This study has been completed.
Genpharm ULC
Information provided by:
Mylan Pharmaceuticals Identifier:
First received: March 30, 2008
Last updated: March 31, 2008
Last verified: March 2008
No Study Results Posted on for this Study
  Study Status: This study has been completed.
  Study Completion Date: July 2003
  Primary Completion Date: July 2003 (Final data collection date for primary outcome measure)