# Budesonide

NDC: 0781-7517
Generic name: Budesonide
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20150724

FDA application: ANDA201966

## Active ingredients

- BUDESONIDE: 1 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-7517"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-7517
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4830c0dd-6964-4108-89bc-3af039612b95