Clinical Trials Directory

Trials / Completed

CompletedNCT00652821

Bioavailability Study of Tramadol/APAP Tablets Under Fed Conditions

To Compare the Relative Bioavailability of the Kali's Tramadol APAP Tablets With Ortho-McNeil's Ultracet Tablets Under Fed Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Par Pharmaceutical, Inc. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

To compare the relative bioavailability of Kali and Ortho-McNeil's products

Detailed description

To compare the relative bioavailability of Kali's Tramadol/APAP 37.5mg/325mg with Ortho-McNeil's Ultracet tablets 37.5mg/325mg

Conditions

Interventions

TypeNameDescription
DRUGTramadol/ APAPTablets 37.5mg /325mg
DRUGUltracetTablets, 37.5mg/325mg

Timeline

Start date
2002-05-01
Primary completion
2002-08-01
Completion
2002-08-01
First posted
2008-04-04
Last updated
2017-09-26

Source: ClinicalTrials.gov record NCT00652821. Inclusion in this directory is not an endorsement.