# decitabine

NDC: 47335-361
Generic name: decitabine
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20140124

FDA application: NDA205582

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-361"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-361
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c155d6ba-9a16-406c-919e-65a149689ab9