FDA NDC Directory · JSON-LD · Markdown

Budesonide

NDC 0536-1112 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerRugby Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA078949
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsBUDESONIDE (32 ug/1)
Marketing started20160727
Marketing ended20270630
Package count1

External sources

Source: openFDA. Public-domain (CC0).