CLOBETASOL PROPIONATE
| Brand name | OLUX |
|---|---|
| Active ingredient | CLOBETASOL PROPIONATE |
| Strength | 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Dosage form | AEROSOL, FOAM |
| Route | TOPICAL |
| Modality | Small molecule |
| FDA approval | May 2000 |
| Marketing status | DISCN |
Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the loss of exclusivity; estimates are projections, not legal advice.