FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 60687-596 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED PELLETS

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA206134
Dosage form / routeCAPSULE, COATED PELLETS · ORAL
Active ingredientsBUDESONIDE (3 mg/1)
Marketing started20210309
Package count1

External sources

Source: openFDA. Public-domain (CC0).