Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 207085

ALBUTEROL SULFATE (ALBUTEROL SULFATE)
EQ 0.09MG BASE/INH
Marketing Status: Prescription
Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: ALBUTEROL SULFATE
Dosage Form; Route of Administration: AEROSOL, METERED; INHALATION
Strength: EQ 0.09MG BASE/INH
Reference Listed Drug: No
Reference Standard: No
TE Code: AB1
Application Number: A207085
Product Number: 001
Approval Date: Jun 1, 2021
Applicant Holder Full Name: SANDOZ INC
Marketing Status:  Prescription
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