Active Ingredient: AZELASTINE HYDROCHLORIDE
Proprietary Name: AZELASTINE HYDROCHLORIDE
Dosage Form; Route of Administration: SPRAY, METERED; NASAL
Strength: 0.137MG/SPRAY
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A091444
Product Number: 001
Approval Date: Oct 24, 2014
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
