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: A206306
Product Number: 001
Approval Date: Dec 7, 2015
Applicant Holder Full Name: SOMERSET THERAPEUTICS LLC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information