Active Ingredient: DESONIDE
Proprietary Name: DESONATE
Dosage Form; Route of Administration: GEL; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021844
Product Number: 001
Approval Date: Oct 20, 2006
Applicant Holder Full Name: LEO PHARMA AS
Marketing Status:
Discontinued
Patent and Exclusivity Information
