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Halobetasol Propionate

NDC 70752-119 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerQUAGEN PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213560
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsHALOBETASOL PROPIONATE (.5 mg/g)
Marketing started20201006
Package count2

External sources

Source: openFDA. Public-domain (CC0).