NDA 21708, held by Somerset. Selegiline.
As of Nov 14, 2026, NDA 21708 (Emsam), held by Somerset, was first approved by FDA on Feb 27, 2006, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Feb 27, 2006 | Original applicationTYPE 6 · Standard review | Approved |
| Emsam6MG · system; transdermal | Selegiline | Rx |
| Emsam9MG · system; transdermal | Selegiline | Rx |
| Emsam12MG · system; transdermal | Selegiline | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters