NDC11 57582021302
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 |
|---|---|
| 57582-0213-02 | 57582-0213 |
| 57582-0213-2 | 57582-0213 |
| 57582-213-02 | 57582-213 |
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 | Tianjin Tianyao Pharmaceuticals Co., Ltd. | 76f9bcb7-0e94-485f-816d-61d4e1ed24e0 | 2022-02-28 | Boxed warning, Warnings, Adverse reactions | 57582-213-02 57582-213 57582021302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.