FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 60505-6129 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA078949
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsBUDESONIDE (32 ug/1)
Marketing started20160419
Package count3

External sources

Source: openFDA. Public-domain (CC0).