NDC11 81469022305
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 |
|---|---|
| 81469-0223-05 | 81469-0223 |
| 81469-0223-5 | 81469-0223 |
| 81469-223-05 | 81469-223 |
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 |
|---|---|---|---|---|---|---|
| Bumetanide | BUMETANIDE | First Nation Group, LLC | 79b77945-74a7-4cb5-8aa0-33a7babdf6d9 | 2026-02-19 | Boxed warning, Warnings, Adverse reactions | 81469-223-05 81469-223 81469022305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.