Active Ingredient: DESONIDE
Proprietary Name: DESONIDE
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.05%
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209996
Product Number: 001
Approval Date: Sep 15, 2017
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information