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ULTRAVATE (HALOBETASOL PROPIONATE) — FDA Approval NDA208183 (LACER PHARMA)

ULTRAVATE (HALOBETASOL PROPIONATE) — FDA Approval NDA208183 (LACER PHARMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ULTRAVATE; Active ingredients: HALOBETASOL PROPIONATE; Application number: NDA208183.

Brand nameULTRAVATE
Active ingredientsHALOBETASOL PROPIONATE
Application numberNDA208183
SponsorLACER PHARMA
Dosage formLOTION
RouteTOPICAL
Marketing statusPrescription
Products in application1
First approval date20151106
SourceopenFDA Drugs@FDA

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