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Active Ingredient: FLUNISOLIDE
Proprietary Name: FLUNISOLIDE
Dosage Form; Route of Administration: SPRAY, METERED; NASAL
Strength: 0.025MG/SPRAY
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A074805
Product Number: 001
Approval Date: Feb 20, 2002
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:
Prescription
Patent and Exclusivity Information