Skyrizi

Product NDC
0074-8350
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
risankizumab-rzaa
Dosage form
INJECTION
Route
SUBCUTANEOUS
Labeler
AbbVie Inc.
Application
BLA761105
Marketing category
BLA
Substance
RISANKIZUMAB
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0074-8350-012 SYRINGE in 1 CARTON (0074-8350-01) / 1.2 mL in 1 SYRINGE2025-09-03NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SkyriziAbbVie Inc.2026-03-19HUMAN PRESCRIPTION DRUG LABEL173