NDC Product Labeler Beone Medicines Usa, Inc.

Beone Medicines Usa, Inc. labeler's code is 72579. The labeler has 11 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
72579-011	Brukinsa	Zanubrutinib	Capsule	Oral	Human Prescription Drug	ACTIVE
72579-015	Beqalzi	Sonrotoclax	Kit		Human Prescription Drug	ACTIVE
72579-017	Beqalzi	Sonrotoclax	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72579-020	Beqalzi	Sonrotoclax	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72579-022	Beqalzi	Sonrotoclax	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72579-025	Beqalzi	Sonrotoclax	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72579-121	Tevimbra	Tislelizumab-jsgr	Injection, Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
72579-122	Brukinsa	Zanubrutinib	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72579-125	Tevimbra	Tislelizumab-jsgr	Injection, Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
72579-901		Zanubrutinib	Tablet, Film Coated		Drug For Further Processing	UNFINISHED
72579-999		Sonrotoclax	Tablet, Film Coated		Drug For Further Processing	UNFINISHED