40
Participants
Start Date
October 31, 2006
Primary Completion Date
October 31, 2006
Study Completion Date
October 31, 2006
Oxycodone HCl 5 mg / Ibuprofen 400 mg tablets, single dose
A: Experimental SSubjects received Actavis formulated products under non-fasting conditions
COMBONOX® tablets, single dose
B: Active comparator Subjects received Forest Pharmaceuticals, Inc formulated products under non-fasting conditions
Gateway Medical Research, Inc, Saint Charles
Lead Sponsor
Actavis Inc.
INDUSTRY