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Beone Medicines Usa, Inc. NDCs and Package Codes

This page lists NDC package records associated with labeler code 72579 (Beone Medicines Usa, Inc.) — including active listings, ingredients, drug names, strengths, dosage forms, package sizes, pricing data when available, and links to each individual NDC page.

Key stats

18
Package NDCs
14
Products
14
Active listings
0
Discontinued
3
Ingredients
0
Therapeutic classes
4
Dosage forms
0
With NADAC pricing

Portfolio

Top ingredients
zanubrutinib 5
sonrotoclax 5
tislelizumab-jsgr 4
By dosage form
TABLET, FILM COATED 6
INJECTION, SOLUTION, CONCENTRATE 4
CAPSULE 3
KIT 1

Browse records — 14 products

Drug / product Billing NDC NADAC / unit Status
BEQALZI sonrotoclax 20 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0025-01 · 1 BLISTER PACK in 1 CARTON (72579-025-01) / 11 TABLET, FILM COATED in 1 BLISTER PACK 72579-0025-01 — On market View →
BEQALZI sonrotoclax KIT BeOne · NDC 72579-0015-04 · 1 KIT in 1 KIT (72579-015-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-017-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-025-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-022-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK 72579-0015-04 — On market View →
BEQALZI sonrotoclax 1 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0020-01 · 1 BLISTER PACK in 1 CARTON (72579-020-01) / 11 TABLET, FILM COATED in 1 BLISTER PACK 72579-0020-01 — On market View →
BEQALZI sonrotoclax 5 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0017-01 · 1 BLISTER PACK in 1 CARTON (72579-017-01) / 11 TABLET, FILM COATED in 1 BLISTER PACK 72579-0017-01 — On market View →
BEQALZI sonrotoclax 80 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0022-01 · 1 BLISTER PACK in 1 CARTON (72579-022-01) / 11 TABLET, FILM COATED in 1 BLISTER PACK 72579-0022-01 — On market View →
BRUKINSA zanubrutinib 80 mg/1 CAPSULE BeOne · NDC 72579-0011-02 · 1 BOTTLE, PLASTIC in 1 CARTON (72579-011-02) / 120 CAPSULE in 1 BOTTLE, PLASTIC 72579-0011-02 — On market View →
BRUKINSA zanubrutinib 160 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0122-01 · 1 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLE 72579-0122-01 — On market View →
BRUKINSA zanubrutinib 160 mg/1 TABLET, FILM COATED BeOne · NDC 72579-0122-01 · 1 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLE 72579-0122-01 — On market View →
BRUKINSA zanubrutinib 80 mg/1 CAPSULE BeOne · NDC 72579-0011-02 · 1 BOTTLE, PLASTIC in 1 CARTON (72579-011-02) / 120 CAPSULE in 1 BOTTLE, PLASTIC 72579-0011-02 — On market View →
TEVIMBRA tislelizumab-jsgr 10 mg/mL INJECTION, SOLUTION, CONCENTRATE BeOne · NDC 72579-0121-01 · J9329 · 1 VIAL, GLASS in 1 CARTON (72579-121-01) / 10 mL in 1 VIAL, GLASS 72579-0121-01 — On market View →
TEVIMBRA tislelizumab-jsgr 10 mg/mL INJECTION, SOLUTION, CONCENTRATE BeOne · NDC 72579-0125-00 · 1 VIAL, GLASS in 1 CARTON (72579-125-00) / 15 mL in 1 VIAL, GLASS 72579-0125-00 — On market View →
TEVIMBRA tislelizumab-jsgr 10 mg/mL INJECTION, SOLUTION, CONCENTRATE BeOne · NDC 72579-0121-01 · J9329 · 1 VIAL, GLASS in 1 CARTON (72579-121-01) / 10 mL in 1 VIAL, GLASS 72579-0121-01 — On market View →
TEVIMBRA tislelizumab-jsgr 10 mg/mL INJECTION, SOLUTION, CONCENTRATE BeOne · NDC 72579-0125-00 · 1 VIAL, GLASS in 1 CARTON (72579-125-00) / 15 mL in 1 VIAL, GLASS 72579-0125-00 — On market View →
zanubrutinib 80 mg/1 CAPSULE BeOne · NDC 72579-0900-01 · 1 BAG in 1 DRUM (72579-900-01) / 20223 CAPSULE in 1 BAG 72579-0900-01 — On market View →
Where does this data come from?
NDC package records, ingredients, strengths and forms come from the openFDA NDC Directory, grouped by the 5-digit labeler code; pricing is CMS NADAC. This is a factual data directory, not a manufacturer marketing page.