# Idarubicin Hydrochloride

NDC: 0143-9217
Generic name: Idarubicin Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20170130

FDA application: ANDA065275

## Active ingredients

- IDARUBICIN HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9217"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9217
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b9b337d5-50f7-4ea9-9df4-72c86e4c0b91