Active Ingredient: LEVOBUNOLOL HYDROCHLORIDE
Proprietary Name: LEVOBUNOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075475
Product Number: 001
Approval Date: Aug 3, 2000
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Discontinued
Patent and Exclusivity Information