NDC11 51672214603
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 |
|---|---|
| 51672-2146-03 | 51672-2146 |
| 51672-2146-3 | 51672-2146 |
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 |
|---|---|---|---|---|---|---|
| IBUPROFEN Infants | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | bc816597-a85a-4143-9f99-bb0699ca57c5 | 2026-03-23 | Warnings | 51672-2146-3 51672-2146 51672214603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.