Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019967

ULTRAVATE (HALOBETASOL PROPIONATE)
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Marketing Status: Discontinued
Active Ingredient: HALOBETASOL PROPIONATE
Proprietary Name: ULTRAVATE
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019967
Product Number: 001
Approval Date: Dec 27, 1990
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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