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Bioavailability Study of Propranolol Under Fed Conditions

To Determine Bioequivalence Under Fed Conditions Clinical Trial

Official title:
Comparative, Randomized, Single-Dose, 2 Way Cross Over Bioavailability Study of Par Propranolol 160 mg With That of Inderal-LA Propranolol 160 mg in Healthy Subjects Under Fed Conditions.

Clinical Trial Summary

To compare the single-dose bioavailability of Propranolol 160 Mg ER Capsules with Inderal-La

Clinical Trial Description

To compare the single -dose bioavailability of Par Propranolol 160 Mg ER capsules with Wyeth Pharmaceuticals, Inderal-LA, Propranolol under fed conditions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00652600
Study type Interventional
Source Par Pharmaceutical, Inc.
Contact
Status Completed
Phase Phase 1
Start date September 2005
Completion date December 2005
View Details
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