Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020688

PATADAY TWICE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)
EQ 0.1% BASE
Marketing Status: Over-the-counter
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

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