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Clobetasol Propionate

NDC 68462-530 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA208933
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsCLOBETASOL PROPIONATE (.5 mg/g)
Marketing started20170320
Package count4

External sources

Source: openFDA. Public-domain (CC0).