Active Ingredient: AZELASTINE HYDROCHLORIDE
Proprietary Name: AZELASTINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.05%
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A078621
Product Number: 001
Approval Date: Aug 3, 2009
Applicant Holder Full Name: APOTEX INC RICHMOND HILL
Marketing Status:
Prescription
Patent and Exclusivity Information