NDC11 00074379902
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 |
|---|---|
| 00074-3799-02 | 00074-3799 |
| 00074-3799-2 | 00074-3799 |
| 0074-3799-02 | 0074-3799 |
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 |
|---|---|---|---|---|---|---|
| Humira | ADALIMUMAB | AbbVie Inc. | 608d4f0d-b19f-46d3-749a-7159aa5f933d | 2025-12-23 | Boxed warning, Warnings, Adverse reactions | 0074-3799-02 0074-3799 00074379902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.