Active Ingredient: DEXAMETHASONE SODIUM PHOSPHATE
Proprietary Name: DEXACORT
Dosage Form; Route of Administration: AEROSOL; NASAL
Strength: EQ 0.1MG PHOSPHATE/INH
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N014242
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: UCB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
