# ONUREG

NDC: 59572-730
Generic name: azacitidine
Labeler / Manufacturer: Celgene Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200901

FDA application: NDA214120

## Active ingredients

- AZACITIDINE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59572-730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59572-730
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e95e33f-8aba-4f19-b332-2416580d358b