NDC11 79481042301
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 |
|---|---|
| 79481-0423-01 | 79481-0423 |
| 79481-0423-1 | 79481-0423 |
| 79481-423-01 | 79481-423 |
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 |
|---|---|---|---|---|---|---|
| pain relief | IBUPROFEN | Meijer, Inc. | ae39917e-1998-4298-8686-919c0d3c2b07 | 2025-09-19 | Warnings | 79481-0423-1 79481-0423 79481042301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.