# IMULDOSA

NDC: 69448-017
Generic name: ustekinumab-srlf
Labeler / Manufacturer: Accord BioPharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20241014

FDA application: BLA761364

## Active ingredients

- USTEKINUMAB-SRLF: 45 mg/.5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69448-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69448-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2539a6cf-0fe5-1565-e063-6294a90a3618