NDC11 24338027001
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 24338-0270-01 | 24338-0270 |
| 24338-0270-1 | 24338-0270 |
| 24338-270-01 | 24338-270 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| VIVIMUSTA | BENDAMUSTINE HYDROCHLORIDE | Azurity Pharmaceuticals, Inc. | 4df6548f-c4ad-4eb2-a54f-19766a3d90ca | 2025-04-03 | Warnings, Adverse reactions | 24338-270-01 24338-270 24338027001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.