# Decitabine

NDC: 72205-031
Generic name: Decitabine
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190828

FDA application: ANDA212265

## Active ingredients

- DECITABINE: 50 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae6c4580-3a3a-4c42-903a-1565d79521f8