FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 64980-638 · HUMAN PRESCRIPTION DRUG · INHALANT

Generic nameBUDESONIDE
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078202
Dosage form / routeINHALANT · RESPIRATORY (INHALATION)
Active ingredientsBUDESONIDE (.25 mg/2mL)
Marketing started20250314
Package count1

External sources

Source: openFDA. Public-domain (CC0).