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BUDESONIDE

NDC 45802-627 · HUMAN PRESCRIPTION DRUG · AEROSOL, FOAM

Generic namebudesonide
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA215328
Dosage form / routeAEROSOL, FOAM · RECTAL
Active ingredientsBUDESONIDE (2 mg/1)
Marketing started20230417
Package count1

External sources

Source: openFDA. Public-domain (CC0).