NDC11 31722036910
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 |
|---|---|
| 31722-0369-10 | 31722-0369 |
| 31722-369-10 | 31722-369 |
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 | Camber Pharmaceuticals, Inc. | 084b34ad-36ba-43bd-a43a-1f4b4da26d8f | 2025-04-14 | Boxed warning, Warnings, Adverse reactions | 31722-369-10 31722-369 31722036910 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.