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FDA Drug Approval, A207085, ALBUTEROL SULFATE
FDA Drug Approval, A207085, ALBUTEROL SULFATE
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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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