# BRUKINSA

NDC: 72579-011
Generic name: zanubrutinib
Labeler / Manufacturer: BeOne Medicines USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20191114

FDA application: NDA213217

## Active ingredients

- ZANUBRUTINIB: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72579-011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72579-011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e08fe23-d70e-424c-bc51-1222e320f902