Active Ingredient: OLOPATADINE HYDROCHLORIDE
Proprietary Name: PATADAY TWICE DAILY RELIEF
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.1% BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N020688
Product Number: 001
Approval Date: Dec 18, 1996
Applicant Holder Full Name: ALCON LABORATORIES INC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
