Sold as Navane. Every FDA application for this active ingredient: 1 branded and 17 generic.
As of Nov 13, 2026, FDA lists 18 applications for Thiothixene (sold as Navane), first approved Jul 24, 1967, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Thiothixene | Part D | $2.1M | -9% | 2,795 |
| Approved | Application | Sponsor | Supplements | Marketing |
|---|---|---|---|---|
| Jul 24, 1967 | NavaneNDA 16584 · New molecular entity | Pfizer | 28 | Discontinued |
| Jun 5, 1987 | ThiothixeneANDA 70600 | Chartwell Rx | 14 | Discontinued |
| Jun 5, 1987 | ThiothixeneANDA 70601 | Chartwell Rx | 15 | Discontinued |
| Jun 5, 1987 | ThiothixeneANDA 70602 | Chartwell Rx | 14 | Discontinued |
| Jun 5, 1987 | ThiothixeneANDA 70603 | Chartwell Rx | 14 | Discontinued |
| Jun 23, 1987 | ThiothixeneANDA 71093 | Rising | 16 | Marketed |
| Jun 24, 1987 | ThiothixeneANDA 71529 | Epic Pharma LLC | 20 | Discontinued |
| Jun 24, 1987 | ThiothixeneANDA 71530 | Sandoz | 18 | Discontinued |
| Apr 5, 2019 | ThiothixeneANDA 211642 | Novitium Pharma | 1 | Marketed |
| Feb 28, 2022 | ThiothixeneANDA 215456 | Amneal | 1 | Marketed |
| — | ThiothixeneANDA 71626 | Watson Labs | 0 | Discontinued |
| — | ThiothixeneANDA 71627 | Watson Labs | 0 | Discontinued |
| — | ThiothixeneANDA 71628 | Watson Labs | 0 | Discontinued |
| — | ThiothixeneANDA 71884 | Am Therap | 0 | Discontinued |
| — | ThiothixeneANDA 71885 | Am Therap | 0 | Discontinued |
| — | ThiothixeneANDA 71886 | Am Therap | 0 | Discontinued |
| — | ThiothixeneANDA 71887 | Am Therap | 0 | Discontinued |
| — | ThiothixeneANDA 72200 | Am Therap | 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