Bendamustine Hydrochloride Injection, Solution
Category: Oncology
FDA status: To Be Discontinued · Last FDA update: Jul 23, 2026 · First posted: Jul 23, 2026 · 1 manufacturers, 1 listed presentations
As of Jul 23, 2026, the FDA lists Bendamustine Hydrochloride Injection, Solution as being discontinued. Of 1 manufacturer presentations, 1 Not specified.
| Presentation & package NDC | Manufacturer | Availability | FDA note |
|---|---|---|---|
| Treanda, Injection, Solution, 25 mg/5 mL, 1 vial, Single-Dose in 1 carton (NDC 63459-390-08) NDC 63459-390-08 |
Cephalon, LLC (a wholly owned subsidiary of Teva Pharmaceutical Industries, Ltd.) | Not specified | A business decision has been made to discontinue manufacture of the drug. |
Related medications in shortage
Other Oncology 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 Bendamustine Hydrochloride Injection, Solution (FDA data as of Jul 23, 2026). Shortage Watch, openFDA.”
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FDA data last synced Oct 1, 2026 (FDA record dated Sep 30, 2026).