Ustekinumab-aekn

Product NDC
51759-709
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ustekinumab-aekn
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
Teva Pharmaceuticals USA, Inc.
Application
BLA761343
Marketing category
BLA
Substance
USTEKINUMAB-AEKN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
51759-709-321 TRAY in 1 CARTON (51759-709-32) / 1 SYRINGE, GLASS in 1 TRAY / .5 mL in 1 SYRINGE, GLASS2025-06-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ustekinumab-aeknTeva Pharmaceuticals USA, Inc.2025-12-03HUMAN PRESCRIPTION DRUG LABEL9