FDA NDC Directory · JSON-LD · Markdown

budesonide

NDC 70771-1075 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED PELLETS

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206134
Dosage form / routeCAPSULE, COATED PELLETS · ORAL
Active ingredientsBUDESONIDE (3 mg/1)
Marketing started20170608
Package count6

External sources

Source: openFDA. Public-domain (CC0).