# Budesonide

NDC: 0487-9601
Generic name: BUDESONIDE
Labeler / Manufacturer: Nephron Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INHALANT
Routes: RESPIRATORY (INHALATION)
Marketing started: 20131001

FDA application: ANDA078202

## Active ingredients

- BUDESONIDE: .25 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0487-9601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0487-9601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f12043df-f9a3-4edb-88f8-dd176c1a141c