NDC11 24208031425
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 |
|---|---|
| 24208-0314-25 | 24208-0314 |
| 24208-314-25 | 24208-314 |
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 |
|---|---|---|---|---|---|---|
| Flurbiprofen Sodium | FLURBIPROFEN SODIUM | Bausch & Lomb Incorporated | 11db354f-caf9-4567-811e-6c9beb1330c7 | 2024-07-24 | Warnings, Adverse reactions | 24208-314-25 24208-314 24208031425 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.