Treats plaque psoriasis of up to 20% body surface area involvement. Sold as Tazorac, Avage, Fabior, Arazlo. Every FDA application for this active ingredient: 4 branded and 10 generic.
As of Nov 15, 2026, FDA lists 14 applications for Tazarotene (sold as Tazorac, Avage, Fabior and others), first approved Jun 13, 1997, with 2 new uses approved and 0 published complete response letters.
| Tazarotene | Part D | $3.2M | +35% | 7,340 |
| Tazorac | Part D | $607K | -58% | 176 |
| Arazlo | Part D | $321K | -9% | 342 |
| Fabior | Part D | $44K | +30% | 12 |
| Jun 13, 1997 | TazoracNDA 20600 · New molecular entity | Chartwell Rx | 7 | Marketed |
| Sep 29, 2000 | Tazorac, AvageNDA 21184 · New dosage form | Chartwell Rx | 5 | Marketed |
| May 11, 2012 | FabiorNDA 202428 · New dosage form | Mayne Pharma | 0 | Marketed |
| Apr 3, 2017 | TazaroteneANDA 208258 | Sun Pharma Canada | 0 | Marketed |
| Dec 22, 2017 | TazaroteneANDA 208662 | Cosette Pharms Nc | 1 | Marketed |
| Jan 28, 2019 | TazaroteneANDA 211175 | Fougera Pharms Inc | 0 | Discontinued |
| Dec 18, 2019 | ArazloNDA 211882 · New formulation or manufacturer | Bausch | 0 | Marketed |
| Sep 13, 2022 | TazaroteneANDA 214136 | Cosette Pharms Nc | 0 | Marketed |
| Sep 13, 2022 | TazaroteneANDA 215433 | Cosette Pharms Nc | 0 | Marketed |
| Mar 20, 2023 | TazaroteneANDA 213644 | Solaris Pharma Corp | 0 | Marketed |
| Apr 25, 2023 | TazaroteneANDA 213079 | Padagis Israel | 0 | Marketed |
| Jul 15, 2024 | TazaroteneANDA 217075 | Padagis Israel | 0 | Marketed |
| Jul 29, 2025 | TazaroteneANDA 215393 | Padagis Israel | 0 | Discontinued |
| Nov 24, 2025 | TazaroteneANDA 214560 | Solaris Pharma Corp | 0 | 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