NDA 221059, held by Azurity Pharmaceuticals Inc. Edaravone.
As of Nov 13, 2026, NDA 221059 (Edaravone), held by Azurity Pharmaceuticals Inc, was not approved, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jul 17, 2026 | Original applicationNew dosage form · Standard review | Tentative approval |
| Product | Active ingredient | Marketing |
|---|---|---|
| Edaravone105MG/5ML · solution;oral | Edaravone | None (tentative approval) |
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