NDC11 27808029701
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 |
|---|---|
| 27808-0297-01 | 27808-0297 |
| 27808-0297-1 | 27808-0297 |
| 27808-297-01 | 27808-297 |
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 | Cranbury Pharmaceuticals, LLC | 933532fa-044a-48b1-bbe4-28062564f98a | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 27808-297-01 27808-297 27808029701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.