# Azacitidine

NDC: 31722-365
Generic name: Azacitidine
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20241015

FDA application: ANDA215765

## 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:"31722-365"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-365
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f02c9bef-e47f-4b70-95f6-9341d87346ed