FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 63629-8294 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA206200
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsBUDESONIDE (3 mg/1)
Marketing started20170915
Package count1

External sources

Source: openFDA. Public-domain (CC0).