NDA 18166, held by Novartis. Oxprenolol Hydrochloride.
As of Nov 13, 2026, NDA 18166 (Trasicor), held by Novartis, was not approved, with 0 approved supplements and 0 published complete response letters.
| Product | Active ingredient | Marketing |
|---|---|---|
| Trasicor20MG · capsule;oral | Oxprenolol Hydrochloride | Discontinued |
| Trasicor40MG · capsule;oral | Oxprenolol Hydrochloride | Discontinued |
| Trasicor80MG · capsule;oral | Oxprenolol Hydrochloride | Discontinued |
| Trasicor160MG · capsule;oral | Oxprenolol Hydrochloride | 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