General MedicationsINHALATIONGeneric
PROVENTIL
ALBUTEROL
Standard Dose
0.09MG/INH
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Discontinued
Summary
Approval overview PROVENTIL is listed in Drugs@FDA under application 017559 (NDA).
Review priority: PRIORITY Marketing status: Discontinued Active ingredient ALBUTEROL Form and strength AEROSOL, METERED;INHALATION - 0.09MG/INH Sponsor SCHERING Submission history Latest submission status date: 2006-09-07 00:00:00.
Structured Monograph
Clinical summary
Approval overview PROVENTIL is listed in Drugs@FDA under application 017559 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient ALBUTEROL Form and strength AEROSOL, METERED;INHALATION - 0.09MG/INH Sponsor SCHERING Submission history Latest submission status date: 2006-09-07 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: PRIORITY
Interaction Notes
- No interaction notes stored yet.