# budesonide

NDC: 68682-658
Generic name: budesonide
Labeler / Manufacturer: Oceanside Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: AEROSOL, FOAM
Routes: RECTAL
Marketing started: 20220715

FDA application: NDA205613

## Active ingredients

- BUDESONIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68682-658"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68682-658
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2cf85c5-3ae0-4f91-9f3a-1d6771e14a73