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Budesonide

NDC 0487-9601 · HUMAN PRESCRIPTION DRUG · INHALANT

Generic nameBUDESONIDE
Labeler / ManufacturerNephron Pharmaceuticals Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA078202
Dosage form / routeINHALANT · RESPIRATORY (INHALATION)
Active ingredientsBUDESONIDE (.25 mg/2mL)
Marketing started20131001
Package count2

External sources

Source: openFDA. Public-domain (CC0).