NDC11 50844075409
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 |
|---|---|
| 50844-0754-09 | 50844-0754 |
| 50844-0754-9 | 50844-0754 |
| 50844-754-09 | 50844-754 |
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 | IBUPROFEN | L.N.K. International, Inc. | 8b5eec38-bdf3-4f27-802f-f4c732ae5c7d | 2026-02-02 | Warnings | 50844-754-09 50844-754 50844075409 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.