A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting Conditions

PHASE1CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

June 30, 2004

Primary Completion Date

July 31, 2004

Study Completion Date

July 31, 2004

Conditions
Healthy
Interventions
DRUG

Abrika Bupropion 150 mg XL Tablet, single dose

A: Experimental Subjects received Abrika formulated products under fasting conditions

DRUG

Wellbutrin XL® 150 mg Tablet, single dose

B: Active comparator Subjects received GlaxoSmithKline formulated products under fasting conditions

Trial Locations (1)

33901

SFBC Ft. Myers, Inc., Fort Myers

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Actavis Inc.

INDUSTRY

NCT00863941 - A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting Conditions | Biotech Hunter | Biotech Hunter