Active Ingredient: CLOBETASOL PROPIONATE
Proprietary Name: OLUX
Dosage Form; Route of Administration: AEROSOL, FOAM; TOPICAL
Strength: 0.05%
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021142
Product Number: 001
Approval Date: May 26, 2000
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
