drugset / Trial / NCT00648713
Fed Study of Terbinafine Hydrochloride Tablets 250 mg and Lamisil® 250 mg
RandomizedCrossoverOpen-labelOther
Summary
The objective of this study was to investigate the bioequivalence of Mylan's terbinafine hydrochloride tablets to Novartis' Lamisil® tablets following a single, oral 250 mg (1 x 250 mg) dose administered under fed conditions.
Timeline
- Start
- 2004-02
- Primary completion
- 2004-03
- Completion
- 2004-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Terbinafine | Small molecule | 250 mg | Oral |
Indications
No indication recorded.