Active Ingredient: LEVOBETAXOLOL HYDROCHLORIDE
Proprietary Name: BETAXON
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: EQ 0.5% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N021114
Product Number: 001
Approval Date: Feb 23, 2000
Applicant Holder Full Name: ALCON PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
