General MedicationsORALStandard
BOSULIF
BOSUTINIB MONOHYDRATE
Standard Dose
EQ 400MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary
Approval overview BOSULIF is listed in Drugs@FDA under application 203341 (NDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient BOSUTINIB MONOHYDRATE Form and strength TABLET;ORAL - EQ 400MG BASE Sponsor PF PRISM CV Submission history Latest submission status date: 2026-03-02 00:00:00.
Structured Monograph
Clinical summary
Approval overview BOSULIF is listed in Drugs@FDA under application 203341 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient BOSUTINIB MONOHYDRATE Form and strength TABLET;ORAL - EQ 400MG BASE Sponsor PF PRISM CV Submission history Latest submission status date: 2026-03-02 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.