# Daunorubicin Hydrochloride

NDC: 42658-021
Generic name: daunorubicin hydrochloride
Labeler / Manufacturer: Hisun Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200120

FDA application: ANDA208759

## Active ingredients

- DAUNORUBICIN HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42658-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42658-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9705fa12-499e-41a3-8fb4-f6df0858b851