Clinical Trials Logo
  1. Home
  2. Other
  3. NCT00652600

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
See also
  Status Clinical Trial Phase
Completed NCT01380496 - Bioequivalence Study of Doxycycline Monohydrate Tablets Under Fed Conditions Phase 1
Completed NCT00652821 - Bioavailability Study of Tramadol/APAP Tablets Under Fed Conditions Phase 1
Completed NCT00652873 - Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fed Conditions Phase 1
Completed NCT00652704 - Bioavailability Study of Doxycycline Monohydrate Capsules and Monodox Under Fasting and Fed Conditions Phase 1
Completed NCT00652730 - Bioavailability Study of (Buspar) Buspirone HCl Tablets Under Fasting and Fed Conditions Phase 1
Completed NCT05329857 - The Study Intends to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossover Design Study Healthy Volunteers. Additionally, the Safety Profile of Test Product Compared to Reference Product Will be Evaluated. N/A
Completed NCT05337969 - The Study Aims to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossover Design Study Healthy Volunteers. Additionally, the Safety Profile of Test Product Compared to Reference Product Will be Assessed. N/A
Completed NCT00653003 - Bioavailability Study of Leflunomide Tablets Under Fed Conditions Phase 1
Completed NCT01380431 - A Comparative Bioavailability Study of Lisinopril Tablets, 40 mg - Effect of Food Study Phase 1