# Dexrazoxane

NDC: 0143-9247
Generic name: Dexrazoxane
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20050331

FDA application: ANDA076068

## Active ingredients

- DEXRAZOXANE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9247"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9247
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=68089182-d4a2-4053-8d0d-fc97a901515d