# DECITABINE

NDC: 75834-190
Generic name: decitabine
Labeler / Manufacturer: Nivagen Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20201217

FDA application: ANDA212117

## Active ingredients

- DECITABINE: 50 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75834-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75834-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=150537a8-10ac-422d-bf33-68b1a408e566