General MedicationsORALStandard
DAYPRO
OXAPROZIN
Standard Dose
600MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary
Approval overview DAYPRO is listed in Drugs@FDA under application 018841 (NDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient OXAPROZIN Form and strength TABLET;ORAL - 600MG Sponsor PFIZER Submission history Latest submission status date: 2024-11-21 00:00:00.
Structured Monograph
Clinical summary
Approval overview DAYPRO is listed in Drugs@FDA under application 018841 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient OXAPROZIN Form and strength TABLET;ORAL - 600MG Sponsor PFIZER Submission history Latest submission status date: 2024-11-21 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.