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UltravateDrug - Ultravate The trade name of the product as shown on the labeling.
Dosage -
OINTMENT; TOPICAL
Active Ingredient(s) -
Halobetasol Propionate
Strength -
0.05%
Applicant -
WESTWOOD SQUIBB
New Drug Application (NDA) Number -
019968
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Dec 17, 1990
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Westwood Squibb Pharmaceuticals Inc
Ultravate
Halobetasol Propionate 0.05% Ointment; Topical
Ultravate 0.05% Ointment; Topical Halog 0.1% Solution; Topical Halobestasol Propionate 0.05% Cream; Topical Halobetasol Propionate 0.05% Cream; Topical Halobetasol Propionate 0.05% Cream; Topical Ultravate 0.05% Cream; Topical Halobetasol Propionate 0.05% Ointment; Topical Halobetasol Propionate 0.05% Ointment; Topical Halobetasol Propionate 0.05% Ointment; Topical NewDrugInformation |