# AZACITIDINE AZACITIDINE

NDC: 43598-678
Generic name: AZACITIDINE
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20171213

FDA application: ANDA207518

## 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:"43598-678"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-678
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d38a1247-28c8-a911-e691-a983a2f9a6e3