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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 212520

UPNEEQ (OXYMETAZOLINE HYDROCHLORIDE)
0.1%
Marketing Status: Prescription
Active Ingredient: OXYMETAZOLINE HYDROCHLORIDE
Proprietary Name: UPNEEQ
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.1%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N212520
Product Number: 001
Approval Date: Jul 8, 2020
Applicant Holder Full Name: RVL PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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