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clobetasol propionate

NDC 68462-625 · HUMAN PRESCRIPTION DRUG · AEROSOL, FOAM

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA211450
Dosage form / routeAEROSOL, FOAM · TOPICAL
Active ingredientsCLOBETASOL PROPIONATE (.5 mg/g)
Marketing started20190909
Package count2

External sources

Source: openFDA. Public-domain (CC0).