Active Ingredient: CARTEOLOL HYDROCHLORIDE
Proprietary Name: CARTEOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A075476
Product Number: 001
Approval Date: Jan 3, 2000
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information