Active Ingredient: FLUNISOLIDE
Proprietary Name: FLUNISOLIDE
Dosage Form; Route of Administration: SPRAY, METERED; NASAL
Strength: 0.025MG/SPRAY
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077704
Product Number: 001
Approval Date: Aug 3, 2006
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:
Prescription
Patent and Exclusivity Information
