FDA Drug Approval, A207085, ALBUTEROL SULFATE

ANDA: 207085
Company: SANDOZ
Drug Name: ALBUTEROL SULFATE
Active Ingredients: ALBUTEROL SULFATE
Strength: EQ 0.09MG BASE/INH
Dosage Form/Route: AEROSOL, METERED;INHALATION
Action Date: 06/01/2021
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB1