NDC11 00002223680
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 |
|---|---|
| 00002-2236-80 | 00002-2236 |
| 0002-2236-80 | 0002-2236 |
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 |
|---|---|---|---|---|---|---|
| Trulicity | DULAGLUTIDE | Eli Lilly and Company | 463050bd-2b1c-40f5-b3c3-0a04bb433309 | 2026-06-16 | Boxed warning, Warnings, Adverse reactions | 0002-2236-80 0002-2236 00002223680 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.