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FDA Approved Drugs·

Approval of Brukinsa, Nda #213217 (Labeling)

Approval Date: 06/04/2024; Drug Name: Brukinsa, Nda #213217; Active Ingredients: ZANUBRUTINIB; Company: Beigene; Submission Status: Approval; Submission Classification: Labeling; Application Number: 213217

Company
BEIGENE
Keywords
BEIGENE