Active Ingredient: CARTEOLOL HYDROCHLORIDE
Proprietary Name: CARTEOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075546
Product Number: 001
Approval Date: Jan 20, 2000
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information