drugset / Trial / NCT00648427

Fasting Study of Paroxetine Hydrochloride Controlled-Release Tablets 25 mg to Paxil CR™ Tablets 25 mg

NCT00648427

Phase 1 Completed 75 enrolled Mylan Pharmaceuticals Inc
RandomizedCrossoverOpen-labelOther

Summary

The objective of this study was to investigate the bioequivalence of Mylan's paroxetine hydrochloride controlled-release 25 mg tablets to GSK's Paxil CR™ 25 mg tablets following a single, oral 25 mg (1 x 25 mg) dose administered under fasting conditions.

Timeline

Start
2005-04
Primary completion
2005-04
Completion
2005-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Paroxetine Small molecule 25 mg Oral

Indications

No indication recorded.