# Budesonide

NDC: 69842-001
Generic name: Budesonide
Labeler / Manufacturer: CVS Pharmacy
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20250701

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:"69842-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69842-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2650d29-c011-48f1-a7f4-040011d4563d