NDA 218820, held by Neurocrine. Crinecerfont.
As of Nov 14, 2026, NDA 218820 (Crenessity), held by Neurocrine, was first approved by FDA on Dec 13, 2024, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Dec 13, 2024 | Original applicationNew dosage form · Priority review | Approved |
| Product | Active ingredient | Marketing |
|---|---|---|
| Crenessity50MG/ML · solution;oral | Crinecerfont | RxReference drug |
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
