FDA NDC Directory · JSON-LD · Markdown

budesonide

NDC 68682-658 · HUMAN PRESCRIPTION DRUG · AEROSOL, FOAM

Labeler / ManufacturerOceanside Pharmaceuticals
Marketing categoryNew Drug Application (innovator) · App NDA205613
Dosage form / routeAEROSOL, FOAM · RECTAL
Active ingredientsBUDESONIDE (2 mg/1)
Marketing started20220715
Package count1

External sources

Source: openFDA. Public-domain (CC0).