NDC11 80425009601
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 |
|---|---|
| 80425-0096-01 | 80425-0096 |
| 80425-0096-1 | 80425-0096 |
| 80425-096-01 | 80425-096 |
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 | b3545cfb-97c3-b896-e053-2a95a90a15a0 | 2024-12-31 | Warnings, Adverse reactions | 80425-0096-1 80425-0096 80425009601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.