# Prolia

NDC: 55513-710
Generic name: denosumab
Labeler / Manufacturer: Amgen, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20100605

FDA application: BLA125320

## 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:"55513-710"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55513-710
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=49e5afe9-a0c7-40c4-af9f-f287a80c5c88