BUTENAFINE HYDROCHLORIDE
| Brand name | LOTRIMIN ULTRA |
|---|---|
| Active ingredient | BUTENAFINE HYDROCHLORIDE |
| Strength | 1% |
| Dosage form | CREAM |
| Route | TOPICAL |
| Modality | Small molecule |
| FDA approval | December 2001 |
| Marketing status | OTC |
Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the loss of exclusivity; estimates are projections, not legal advice.