NDC11 00591367101
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 |
|---|---|
| 00591-3671-01 | 00591-3671 |
| 00591-3671-1 | 00591-3671 |
| 0591-3671-01 | 0591-3671 |
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 |
|---|---|---|---|---|---|---|
| Nabumetone | NABUMETONE | Actavis Pharma, Inc. | 53656d70-6572-4669-6465-6c6973555341 | 2025-07-07 | Boxed warning, Warnings, Adverse reactions | 0591-3671-01 0591-3671 00591367101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.