Active Ingredient: OLOPATADINE HYDROCHLORIDE
Proprietary Name: OLOPATADINE HYDROCHLORIDE
Dosage Form; Route of Administration: SPRAY, METERED; NASAL
Strength: 0.665MG/SPRAY
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A210901
Product Number: 001
Approval Date: Jan 28, 2020
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information