# AZACITIDINE

NDC: 70121-1237
Generic name: AZACITIDINE
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20220209

FDA application: ANDA211549

## Active ingredients

- AZACITIDINE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70121-1237"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70121-1237
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80a43736-0598-4e4b-85ba-e29daa290c8f