A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Non-fasting Conditions

PHASE1CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

December 31, 1997

Primary Completion Date

January 31, 1998

Study Completion Date

January 31, 1998

Conditions
Healthy
Interventions
DRUG

Gabapentin 400 mg capsules

A: Experimental Subjects received Purepac formulated products under fed conditions

DRUG

NEURONTIN® 400 mg capsules

B: Active comparator Subjects received Parke-Davis's marketed product

DRUG

Gabapentin 400 mg capsules, single dose

C: Experimental Subjects received Purepac formulated products under fasting conditions

Trial Locations (1)

63301

Gateway Medical Research, Inc, Saint Charles

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Actavis Inc.

INDUSTRY