Active Ingredient: KETOTIFEN FUMARATE
Proprietary Name: KETOTIFEN FUMARATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.025% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077958
Product Number: 001
Approval Date: Jul 26, 2007
Applicant Holder Full Name: SENTISS AG
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
