Phenoxybenzamine Hydrochloride Capsule
Category: Cardiovascular
FDA status: To Be Discontinued · Last FDA update: Dec 1, 2025 · First posted: Dec 1, 2025 · 1 manufacturers, 3 listed presentations
As of Dec 1, 2025, the FDA lists Phenoxybenzamine Hydrochloride Capsule as being discontinued. Of 3 manufacturer presentations, 3 Not specified.
| Presentation & package NDC | Manufacturer | Availability | FDA note |
|---|---|---|---|
| Dibenzyline, Capsule, 10 mg (NDC 59212-001-02) NDC 59212-001-02 |
Advanz Pharma (US) Corp. | Not specified | Discontinuation of the manufacture of the drug |
| Dibenzyline, Capsule, 10 mg (NDC 59212-001-01) NDC 59212-001-01 |
Advanz Pharma (US) Corp. | Not specified | Discontinuation of the manufacture of the drug |
| Dibenzyline, Capsule, 10 mg (NDC 66993-066-02) NDC 66993-066-02 |
Advanz Pharma (US) Corp. | Not specified | Discontinuation of the manufacture of the drug |
Related medications in shortage
Other Cardiovascular medications currently on the FDA shortage list — useful context if you and your prescriber are weighing alternatives. Always confirm with your pharmacist.
Change log
Tracking began Oct 1, 2026. We check the FDA every 6 hours; any real change - a manufacturer moving from Limited to Available, a new recovery date, a new listing - shows up here with its date.
Cite this: “FDA drug-shortage status for Phenoxybenzamine Hydrochloride Capsule (FDA data as of Dec 1, 2025). Shortage Watch, openFDA.”
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FDA data last synced Oct 1, 2026 (FDA record dated Sep 30, 2026).