risankizumab-rzaa 360 MG per 2.4 ML Cartridge
- RxCUI
- 2604625
- RxNorm name
- risankizumab-rzaa 360 MG per 2.4 ML Cartridge
- Display name
- risankizumab-rzaa 360 MG per 2.4 ML Cartridge
- Full name
- risankizumab-rzaa 360 MG per 2.4 ML Cartridge
- Term type
- SY
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:39:03
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 |
|---|---|---|---|---|---|---|
| Skyrizi | RISANKIZUMAB-RZAA | AbbVie Inc. | 7148c8eb-b39e-e20a-6494-a6df82392858 | 2026-06-15 | Warnings, Adverse reactions | 2604625 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 7148c8eb-b39e-e20a-6494-a6df82392858 | risankizumab-rzaa 360 MG per 2.4 ML Cartridge | SY | 173 | These highlights do not include all the information needed to use SKYRIZI safely and effectively. See full prescribing information for SKYRIZI. SKYRIZI ® (risankizumab-rzaa) injection, for subcutaneous or intravenous use Initial U.S. Approval: 2019 | 20260319 |
| 7148c8eb-b39e-e20a-6494-a6df82392858 | 2.4 ML risankizumab-rzaa 150 MG/ML Cartridge | SCD | 173 | These highlights do not include all the information needed to use SKYRIZI safely and effectively. See full prescribing information for SKYRIZI. SKYRIZI ® (risankizumab-rzaa) injection, for subcutaneous or intravenous use Initial U.S. Approval: 2019 | 20260319 |
| 7148c8eb-b39e-e20a-6494-a6df82392858 | risankizumab-rzaa 360 MG in 2.4 ML Cartridge | PSN | 173 | These highlights do not include all the information needed to use SKYRIZI safely and effectively. See full prescribing information for SKYRIZI. SKYRIZI ® (risankizumab-rzaa) injection, for subcutaneous or intravenous use Initial U.S. Approval: 2019 | 20260319 |