Sold as Navane. Every FDA application for this active ingredient: 2 branded and 6 generic.
As of Nov 15, 2026, FDA lists 8 applications for Thiothixene Hydrochloride (sold as Navane), first approved Apr 6, 1970, with 0 new uses approved and 0 published complete response letters.
| Apr 6, 1970 | NavaneNDA 16758 · New active ingredient | Pfizer | 7 | Discontinued |
| Aug 19, 1971 | NavaneNDA 16904 · New active ingredient | Pfizer | 17 | Discontinued |
| Jun 22, 1987 | Thiothixene HydrochlorideANDA 71184 | Teva | 4 | Discontinued |
| Oct 16, 1987 | Thiothixene HydrochlorideANDA 71554 | Teva Pharms | 14 | Discontinued |
| — | Thiothixene HydrochlorideANDA 70969 | Alpharma US Pharms | 0 | Discontinued |
| — | Thiothixene HydrochlorideANDA 71917 | Paco | 0 | Discontinued |
| — | Thiothixene HydrochlorideANDA 71939 | Paco | 0 | Discontinued |
| — | Thiothixene Hydrochloride IntensolANDA 73494 | Hikma | 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