NDC 72579-025 – Beqalzi

Sonrotoclax 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72579-025

Product details

Brand name
Beqalzi
Generic name
sonrotoclax
Labeler
BeOne Medicines USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA220711
Marketed since
August 31, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Beqalzi →

Package NDC codes (2)

Package NDCDescriptionSince
72579-025-011 BLISTER PACK in 1 CARTON (72579-025-01) / 11 TABLET, FILM COATED in 1 BLISTER PACKAug 31, 2026
72579-025-021 BLISTER PACK in 1 CARTON (72579-025-02) / 14 TABLET, FILM COATED in 1 BLISTER PACKAug 31, 2026

Other Beqalzi products