Clinical Trials Directory

Trials / Completed

CompletedNCT00648401

Food Study of Verapamil HCl Extended-Release Capsules 300 mg and Verelan® PM Extended-Release Capsules 300 mg

Single-Dose Fed Bioequivalence Study of Verapamil HCl Extended-Release Capsules (300 mg; Mylan) and Verelan® PM Extended-Release Capsules (300 mg; Schwarz) in Healthy Volunteers

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

Summary

The objective for this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following a single, oral 300 mg (1 x 300 mg) dose administration under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGVerapamil Hydrochloride Extended-Release Capsules, 300 mg300mg, single dose fed
DRUGVerelan® PM Extended-Release Capsules, 300 mg300mg, single dose fed

Timeline

Start date
2006-01-01
Primary completion
2006-01-01
Completion
2006-02-01
First posted
2008-04-01
Last updated
2024-04-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00648401. Inclusion in this directory is not an endorsement.