drugset / Trial / NCT00648271

Fed Study of Metoprolol Tartrate Tablets 25 mg and Lopressor® 50 mg

NCT00648271

Phase 1 Completed 19 enrolled Mylan Pharmaceuticals Inc
RandomizedCrossoverOpen-labelOther

Summary

The objective of this study was to investigate the bioequivalence of Mylan's metoprolol tartrate tablets to Novartis' Lopressor® tablets following a single, oral 50 mg (2 x 25 mg tablets for Mylan's formulation and 1 x 50 mg for Lopressor®) dose administered under fed conditions.

Timeline

Start
2002-12
Primary completion
2002-12
Completion
2003-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Metoprolol Other / unclassified 50 mg Oral

Indications

No indication recorded.