Overview

Ursodiol Tablets 500 mg Under Fasting Conditions

Status:
Completed
Trial end date:
2007-01-01
Target enrollment:
Participant gender:
Summary
The objective of this study was to evaluate the comparative bioavailability between Ursodiol 500 mg Tablets (test) and Urso Forteā„¢ 500 mg Tablets (reference) after a single-dose in healthy subjects under fasting conditions.
Phase:
Phase 1
Details
Lead Sponsor:
Teva Pharmaceuticals USA
Treatments:
Ursodeoxycholic Acid