Overview

Terbinafine HCl 250 mg Tablet Under Fasting Conditions

Status:
Completed
Trial end date:
2002-01-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the relative bioavailability of the test formulation of terbinafine tablets with an already marketed reference formulation LamisilĀ® (Novartis Pharmaceuticals), under fasted conditions in healthy, non-tobacco using male and female adult subjects.
Phase:
Phase 1
Details
Lead Sponsor:
Teva Pharmaceuticals USA
Treatments:
Terbinafine