Sold as Corgard. Every FDA application for this active ingredient: 1 branded and 14 generic.
As of Nov 14, 2026, FDA lists 15 applications for Nadolol (sold as Corgard), first approved Dec 10, 1979, with 2 new uses approved and 0 published complete response letters.
| Nadolol | Part D | $13.2M | -10% | 62,233 |
| Corgard | Part D | $0K | -100% | 0 |
| MEdical Treatment in Idiopathic Ventricular Fibrillation PatientsIdiopathic Ventricular Fibrillation, Cardiac Arrest, Out-Of-Hospital · Bo Gregers Winkel | Phase 4 | Recruiting | Feb 12, 2026 |
| Pre-emptive RTO for An Early Detected Gastric Varices in CT/MR Angiogram TrialGastric Varices · University of California, Los Angeles | Not applicable | Recruiting | Sep 11, 2025 |
| Exercise as an Immune Adjuvant for Allogeneic Cell TherapiesLeukemia, Hematopoetic Stem Cell Transplantation · University of Arizona | Early phase 1 | Recruiting | Oct 16, 2024 |
| A Preliminary Study for INFORMEDHeart Failure, Heart Failure, Diastolic · Weill Medical College of Cornell University | Phase 4 | Recruiting | Oct 18, 2022 |
| Dec 10, 1979 | CorgardNDA 18063 · New molecular entity | Uswm | 56 | Discontinued |
| Oct 31, 1993 | NadololANDA 74172 | Rising | 6 | Marketed |
| Aug 31, 1994 | NadololANDA 74368 | Teva Pharms | 4 | Discontinued |
| Nov 9, 1995 | NadololANDA 74501 | Sandoz | 5 | Marketed |
| Jan 24, 1996 | NadololANDA 74255 | Heritage Pharma | 9 | Discontinued |
| Aug 30, 1996 | NadololANDA 74229 | Heritage Pharma | 10 | Discontinued |
| Sep 16, 2015 | NadololANDA 201893 | Aurobindo Pharma | 3 | Marketed |
| Dec 18, 2015 | NadololANDA 203455 | Invagen Pharms | 1 | Marketed |
| Jun 2, 2017 | NadololANDA 208832 | Amneal Pharms Co | 1 | Marketed |
| Jul 28, 2017 | NadololANDA 207761 | Zydus Pharms | 1 | Marketed |
| Oct 5, 2017 | NadololANDA 209309 | Chartwell Rx | 0 | Marketed |
| Jun 1, 2018 | NadololANDA 210786 | Ingenus Pharms LLC | 1 | Discontinued |
| Jul 23, 2018 | NadololANDA 210955 | Regcon Holdings | 1 | Marketed |
| Sep 13, 2019 | NadololANDA 212856 | Somerset Theraps LLC | 0 | Marketed |
| Jun 2, 2023 | NadololANDA 211763 | Alembic | 1 | Marketed |
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient. Drugs@FDA