NDA 10520, held by Merck. Anileridine Phosphate.
As of Nov 13, 2026, NDA 10520 (Leritine), held by Merck, was not approved, with 0 approved supplements and 0 published complete response letters.
| Product | Active ingredient | Marketing |
|---|---|---|
| Leritine25MG/ML ยท injectable;injection | Anileridine Phosphate | Discontinued |
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
