# Budesonide

NDC: 63629-8294
Generic name: Budesonide
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20170915

FDA application: ANDA206200

## Active ingredients

- BUDESONIDE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-8294"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-8294
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4943ef5b-f48b-49d6-b419-467f71ef64e0