Drug company (FDA labeler)
BeOne Medicines USA, Inc.
NDC labeler code: 72579
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- SonrotoclaxBeqalzi · 4 products
- Tislelizumab-jsgrTevimbra · 2 products
- ZanubrutinibBrukinsa · 2 products
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| May 13, 2026 | NDA220711 | Sonrotoclax BEQALZI | Beone Medicines USA |
| June 10, 2025 | NDA218785 | Zanubrutinib BRUKINSA | Beone Medicines USA |
| March 13, 2024 | BLA761232 | Tislelizumab-jsgr TEVIMBRA | Beigene |
| November 14, 2019 | NDA213217 | Zanubrutinib BRUKINSA | Beone Medicines USA |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026