# Budesonide

NDC: 0536-1112
Generic name: Budesonide
Labeler / Manufacturer: Rugby Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20160727
Marketing ended: 20270630
FDA application: ANDA078949

## Active ingredients

- BUDESONIDE: 32 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0536-1112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0536-1112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04eb9e98-1323-353f-3fd7-2d317dfac526