FdaApplication

NDA 019968

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeNDA
approval_date1990-12-17

Products (1)

ProductActive ingredientStrengthDosage form
ULTRAVATEHALOBETASOL PROPIONATE0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**OINTMENT;TOPICAL

1 product