Sold as Cartrol, Ocupress. Every FDA application for this active ingredient: 2 branded and 3 generic.
As of Nov 15, 2026, FDA lists 5 applications for Carteolol Hydrochloride (sold as Cartrol, Ocupress), first approved Dec 28, 1988, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Carteolol HCl | Part D | $421K | -7% | 5,171 |
| Dec 28, 1988 | CartrolNDA 19204 · New molecular entity | Abbvie | 2 | Discontinued |
| May 23, 1990 | OcupressNDA 19972 · New dosage form | Novartis | 18 | Discontinued |
| Jan 3, 2000 | Carteolol HydrochlorideANDA 75476 | Sandoz | 5 | Marketed |
| Jan 20, 2000 | Carteolol HydrochlorideANDA 75546 | Bausch And Lomb | 7 | Discontinued |
| Feb 6, 2002 | Carteolol HydrochlorideANDA 76097 | Apotex Inc | 0 | Discontinued |
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