NDC11 00002688530
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 |
|---|---|
| 00002-6885-30 | 00002-6885 |
| 0002-6885-30 | 0002-6885 |
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 |
|---|---|---|---|---|---|---|
| Baricitinib | BARICITINIB | Eli Lilly and Company | 7052c055-fedf-453b-86bc-01f5465eb157 | 2022-05-10 | 0002-6885-30 0002-6885 00002688530 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.