Active Ingredient: OLOPATADINE HYDROCHLORIDE
Proprietary Name: OLOPATADINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.1% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206046
Product Number: 001
Approval Date: Jul 26, 2017
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information