# Azacitidine

NDC: 70069-857
Generic name: Azacitidine
Labeler / Manufacturer: Somerset Therapeutics LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20250829

FDA application: ANDA217453

## Active ingredients

- AZACITIDINE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-857"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-857
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3bc4f406-2ec7-7169-e063-6394a90a81d9