Active Ingredient: LEVOBUNOLOL HYDROCHLORIDE
Proprietary Name: LEVOBUNOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074851
Product Number: 001
Approval Date: Oct 28, 1996
Applicant Holder Full Name: ALCON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
