lecanemab-irmb 360 MG per 1.8 ML Auto-Injector
- RxCUI
- 2723406
- RxNorm name
- lecanemab-irmb 360 MG per 1.8 ML Auto-Injector
- Display name
- lecanemab-irmb 360 MG per 1.8 ML Auto-Injector
- Full name
- lecanemab-irmb 360 MG per 1.8 ML Auto-Injector
- Term type
- SY
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:39:10
Purple Book Biologic Products#
UNII Substances#
No records found.
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 |
|---|---|---|---|---|---|---|
| LEQEMBI | LECANEMAB | Eisai Inc. | 9d1ff786-e577-410a-a273-c4d7d0e4e975 | 2026-07-21 | Boxed warning, Warnings, Adverse reactions | 2723406 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 9d1ff786-e577-410a-a273-c4d7d0e4e975 | lecanemab-irmb 360 MG per 1.8 ML Auto-Injector | SY | 22 | These highlights do not include all the information needed to use LEQEMBI ® safely and effectively. See full prescribing information for LEQEMBI ® . LEQEMBI ® (lecanemab-irmb) injection, for intravenous or subcutaneous use Initial U.S. Approval: 2023 | 20260123 |
| 9d1ff786-e577-410a-a273-c4d7d0e4e975 | lecanemab-irmb 360 MG in 1.8 ML Auto-Injector | PSN | 22 | These highlights do not include all the information needed to use LEQEMBI ® safely and effectively. See full prescribing information for LEQEMBI ® . LEQEMBI ® (lecanemab-irmb) injection, for intravenous or subcutaneous use Initial U.S. Approval: 2023 | 20260123 |
| 9d1ff786-e577-410a-a273-c4d7d0e4e975 | 1.8 ML lecanemab-irmb 200 MG/ML Auto-Injector | SCD | 22 | These highlights do not include all the information needed to use LEQEMBI ® safely and effectively. See full prescribing information for LEQEMBI ® . LEQEMBI ® (lecanemab-irmb) injection, for intravenous or subcutaneous use Initial U.S. Approval: 2023 | 20260123 |