# zanubrutinib

NDC: 72579-901
Generic name: zanubrutinib
Labeler / Manufacturer: BeOne Medicines USA, Inc.
Product type: DRUG FOR FURTHER PROCESSING
Marketing category: DRUG FOR FURTHER PROCESSING
Dosage form: TABLET, FILM COATED
Routes: —
Marketing started: 20260914



## Active ingredients

- ZANUBRUTINIB: 160 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72579-901"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72579-901