Overview

Buprenorphine 8 mg Sublingual Tablets Under Fasting Conditions

Status:
Completed
Trial end date:
2007-09-01
Target enrollment:
Participant gender:
Summary
The object of this study is to compare the rate and extent of absorption of an investigational formulation of buprenorphine 8 mg sublingual tablets manufactured by Barr Laboratories, Inc. to an equivalent oral dose of the commercially available reference product, Subutex® manufactured by Reckitt Benckiser, following and overnight fast of at least 10 hours.
Phase:
Phase 1
Details
Lead Sponsor:
Teva Pharmaceuticals USA
Treatments:
Buprenorphine