Treats hypertension. Sold as Minipress, Minipress Xl. Every FDA application for this active ingredient: 2 branded and 27 generic.
As of Nov 15, 2026, FDA lists 29 applications for Prazosin Hydrochloride (sold as Minipress, Minipress Xl), first approved Jun 23, 1976, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Prazosin HCl | Part D | $25.4M | +1% | 234,011 |
| Assessing Trauma-related Links Between Affective and Metabolic SystemsPosttraumatic Stress Disorder, Metabolic Syndrome · VA Office of Research and Development | Phase 4 | Not yet recruiting | Oct 7, 2026 |
| Brain Blood Vessel Responses to Changes in Blood FlowMagnetic Resonance Imaging, Cerebrovascular Circulation · University of Wisconsin, Madison | Phase 2 | Recruiting | Oct 8, 2024 |
| Brain Blood Vessel Responses to Changes in Blood Flow: Younger CohortMagnetic Resonance Imaging, Cerebrovascular Circulation · University of Wisconsin, Madison | Phase 2 | Recruiting | Oct 8, 2024 |
| Alpha-1 Blockade for Alcohol Use Disorder (AUD)Alcohol Use Disorder (AUD) · Brown University | Phase 2 | Active, not recruiting | Oct 23, 2019 |
| Predicting Responses to PTSD Treatment With Iris and Cardiovascular TestsPosttraumatic Stress Disorder · VA Office of Research and Development | Phase 3 | Active, not recruiting | May 29, 2018 |
| Jun 23, 1976 | MinipressNDA 17442 · New molecular entity | Pfizer | 34 | Marketed |
| Sep 12, 1988 | Prazosin HydrochlorideANDA 71745 | Teva Pharms | 12 | Marketed |
| Sep 12, 1988 | Prazosin HydrochlorideANDA 71994 | Ivax Sub Teva Pharms | 12 | Marketed |
| Sep 12, 1988 | Prazosin HydrochlorideANDA 71995 | Teva Pharms | 13 | Marketed |
| Jan 11, 1989 | Prazosin HydrochlorideANDA 72333 | Watson Labs | 5 | Discontinued |
| Jan 11, 1989 | Prazosin HydrochlorideANDA 72352 | Watson Labs | 5 | Discontinued |
| Jan 11, 1989 | Prazosin HydrochlorideANDA 72609 | Watson Labs | 5 | Discontinued |
| Feb 28, 1989 | Prazosin HydrochlorideANDA 72573 | Mylan | 7 | Marketed |
| Feb 28, 1989 | Prazosin HydrochlorideANDA 72574 | Mylan | 7 | Marketed |
| Feb 28, 1989 | Prazosin HydrochlorideANDA 72575 | Mylan | 10 | Marketed |
| Mar 15, 1989 | Prazosin HydrochlorideANDA 72705 | Dava Pharms Inc | 8 | Discontinued |
| Mar 15, 1989 | Prazosin HydrochlorideANDA 72706 | Dava Pharms Inc | 8 | Discontinued |
| Mar 15, 1989 | Prazosin HydrochlorideANDA 72707 | Dava Pharms Inc | 9 | Discontinued |
| Apr 10, 1989 | Prazosin HydrochlorideANDA 72577 | Ani Pharms | 2 | Discontinued |
| Jan 29, 1992 | Minipress XlNDA 19775 · New dosage form | Pfizer | 2 | Discontinued |
| Oct 3, 2018 | Prazosin HydrochlorideANDA 210971 | Novitium Pharma | 0 | Marketed |
| Dec 23, 2021 | Prazosin HydrochlorideANDA 214608 | Granules | 0 | Marketed |
| Oct 21, 2022 | Prazosin HydrochlorideANDA 213406 | Appco | 0 | Marketed |
| Dec 30, 2022 | Prazosin HydrochlorideANDA 215697 | Mankind Pharma | 0 | Marketed |
| Mar 6, 2023 | Prazosin HydrochlorideANDA 217268 | Alembic | 0 | Marketed |
| Mar 31, 2023 | Prazosin HydrochlorideANDA 213052 | Aurobindo Pharma Ltd | 0 | Marketed |
| Jan 3, 2024 | Prazosin HydrochlorideANDA 214083 | Lannett Co Inc | 0 | Discontinued |
| Sep 17, 2024 | Prazosin HydrochlorideANDA 216727 | Msn | 0 | Marketed |
| — | Prazosin HydrochlorideANDA 72782 | Am Therap | 0 | Discontinued |
| — | Prazosin HydrochlorideANDA 72783 | Am Therap | 0 | Discontinued |
| — | Prazosin HydrochlorideANDA 72784 | Am Therap | 0 | Discontinued |
| — | Prazosin HydrochlorideANDA 72921 | Purepac Pharm | 0 | Discontinued |
| — | Prazosin HydrochlorideANDA 72991 | Purepac Pharm | 0 | Discontinued |
| — | Prazosin HydrochlorideANDA 72992 | Purepac Pharm | 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