# OSVYRTI

NDC: 69448-021
Generic name: denosumab-desu
Labeler / Manufacturer: Accord BioPharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20260706

FDA application: BLA761424

## Active ingredients

- DENOSUMAB: 60 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69448-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69448-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5f3be096-5100-4d0e-b765-481bbb2672e1