# Decitabine

NDC: 68001-642
Generic name: Decitabine
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250501

FDA application: ANDA215355

## 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:"68001-642"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-642
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de303068-589e-4e0a-90ed-e60b2c1a2b56