Active Ingredient: HALOBETASOL PROPIONATE
Proprietary Name: ULTRAVATE
Dosage Form; Route of Administration: OINTMENT; 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Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019968
Product Number: 001
Approval Date: Dec 17, 1990
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
