# SIMPONI ARIA

NDC: 57894-350
Generic name: golimumab
Labeler / Manufacturer: Janssen Biotech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20130719

FDA application: BLA125433

## Active ingredients

- GOLIMUMAB: 50 mg/4mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57894-350"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57894-350
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e260a47-55af-4c92-8d88-a86ccc767fff