Clinical Trials Directory

Trials / Completed

CompletedNCT00647660

Fasting Study of Nadolol/Bendroflumethiazide Tablets 80 mg/5 mg and Corzide® Tablets 80 mg/5 mg

Single-Dose Fasting Bioequivalence Study of Nadolol/Bendroflumethiazide Tablets (80 mg/5 mg; Mylan) to Corzide® Tablets (80 mg/5 mg; King) in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Mylan Pharmaceuticals Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to investigate the bioequivalence of Mylan's nadolol/bendroflumethiazide 80 mg/5 mg tablets to King's Corzide® 80 mg/5 mg tablets following a single, oral 80 mg/5 mg (1 x 80 mg/5 mg) dose administered under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGNadolol/Bendroflumethiazide Tablets 80 mg/5 mg80/5mg, single dose fasting
DRUGCorzide® Tablets 80 mg/5 mg80/5mg, single dose fasting

Timeline

Start date
2006-07-01
Primary completion
2006-08-01
Completion
2006-08-01
First posted
2008-04-01
Last updated
2024-04-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00647660. Inclusion in this directory is not an endorsement.

Fasting Study of Nadolol/Bendroflumethiazide Tablets 80 mg/5 mg and Corzide® Tablets 80 mg/5 mg (NCT00647660) · Clinical Trials Directory