# Budesonide

NDC: 60505-6129
Generic name: Budesonide
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20160419

FDA application: ANDA078949

## Active ingredients

- BUDESONIDE: 32 ug/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-6129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1aac35a-bc72-dd68-8179-8661354589cb