NDC11 50580023004
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 |
|---|---|
| 50580-0230-04 | 50580-0230 |
| 50580-0230-4 | 50580-0230 |
| 50580-230-04 | 50580-230 |
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 |
|---|---|---|---|---|---|---|
| Motrin IB | IBUPROFEN | Kenvue Brands LLC | d21129f8-4d96-4e36-bc39-a534306dd77e | 2025-10-03 | Warnings | 50580-230-04 50580-230 50580023004 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.