# Uceris

NDC: 68012-309
Generic name: budesonide
Labeler / Manufacturer: Santarus Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130114

FDA application: NDA203634

## Active ingredients

- BUDESONIDE: 9 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68012-309"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68012-309
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92cbb190-8851-46ed-bfe0-166ca62ef2e9