drugset / Trial / NCT00871364

A Relative Bioavailability Study of 50 mg Venlafaxine Hydrochloride Tablets Under Fed Conditions

NCT00871364

Phase 1 Completed 30 enrolled Actavis Inc.
RandomizedCrossoverOpen-label

Summary

The purpose of this study to assess the single-dose relative bioavailability of Actavis Group hf 50 mg venlafaxine hydrochloride tablets with Wyeth Pharmaceuticals (Effexor®) 50 mg venlafaxine (as venlafaxine hydrochloride) tablets under fed conditions.

Timeline

Start
2006-04
Primary completion
2006-05
Completion
2006-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Venlafaxine Small molecule 50 mg

Indications

No indication recorded.