NDC11 80425003701
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 |
|---|---|
| 80425-0037-01 | 80425-0037 |
| 80425-0037-1 | 80425-0037 |
| 80425-037-01 | 80425-037 |
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 |
|---|---|---|---|---|---|---|
| Celecoxib | CELECOXIB | Advanced Rx of Tennessee, LLC | af73fea0-5cd1-0fa2-e053-2a95a90af8fc | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 80425-0037-1 80425-0037 80425003701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.