FDA NDC Directory · JSON-LD · Markdown

BEQALZI

NDC 72579-017 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesonrotoclax
Labeler / ManufacturerBeOne Medicines USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA220711
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSONROTOCLAX (5 mg/1)
Marketing started20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).