drugset / Trial / NCT00864760

A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Conditions

NCT00864760

Phase 1 Completed 30 enrolled Actavis Inc.
RandomizedCrossoverOpen-label

Summary

The purpose of this study is to compare the relative bioavailability of 800 mg Gabapentin Tablets by Purepac Pharmaceutical Co. with that of 400 mg (2 x 400 mg) NEURONTIN® by Parke-Davis under fasting conditions.

Timeline

Start
1999-06
Primary completion
1999-06
Completion
1999-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Gabapentin Small molecule 400 mg
Subject Gabapentin Small molecule 800 mg

Indications

No indication recorded.