Treats schizophrenia. Sold as Geodon. Every FDA application for this active ingredient: 1 branded and 3 generic.
As of Nov 15, 2026, FDA lists 4 applications for Ziprasidone Mesylate (sold as Geodon), first approved Jun 21, 2002, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Ziprasidone Mesylate | Part D | $406K | -17% | 1,162 |
| Lumateperone for the Improvement of Apathy in Patients With Psychotic Symptoms.Apathy, Schizophrenia · Louisiana State University Health Sciences Center Shreveport | Phase 3 | Recruiting | Jul 1, 2024 |
| Maternal And Infant Antipsychotic StudyAntipsychotics, Pregnancy · Icahn School of Medicine at Mount Sinai | — | Recruiting | Sep 22, 2023 |
| Proposal To Develop A Rapid And Cost-Effective Diagnostic Test For SchizophreniaSchizophrenia · University of Arizona | Phase 1 | Active, not recruiting | Dec 19, 2018 |
| Jun 21, 2002 | GeodonNDA 20919 · New dosage form | Viatris | 26 | Marketed |
| Dec 26, 2019 | Ziprasidone MesylateANDA 211908 | Gland | 4 | Marketed |
| Sep 15, 2022 | Ziprasidone MesylateANDA 216091 | Msn | 0 | Marketed |
| Sep 3, 2025 | Ziprasidone MesylateANDA 217595 | Steriscience | 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