FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 47335-633 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211922
Dosage form / routeSUSPENSION · RESPIRATORY (INHALATION)
Active ingredientsBUDESONIDE (1 mg/2mL)
Marketing started20210501
Package count1

External sources

Source: openFDA. Public-domain (CC0).