# USTEKINUMAB-AAUZ

NDC: 65219-862
Generic name: ustekinumab-aauz
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20251115

FDA application: BLA761379

## Active ingredients

- USTEKINUMAB: 45 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-862"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-862
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6d75316-c9a7-49cf-83be-b7b6c6cecf7a