Active Ingredient: BETAXOLOL HYDROCHLORIDE
Proprietary Name: BETAXOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.5% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075386
Product Number: 001
Approval Date: Jun 30, 2000
Applicant Holder Full Name: AKORN OPERATING CO LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
