NDC11 70518373301
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 |
|---|---|
| 70518-3733-01 | 70518-3733 |
| 70518-3733-1 | 70518-3733 |
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 | REMEDYREPACK INC. | b3acbfd9-a1c2-4aa6-b5f0-013cfad6cca8 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | 70518-3733-1 70518-3733 70518373301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.