# Doxorubicin Hydrochloride

NDC: 0069-4031
Generic name: Doxorubicin Hydrochloride
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250331

FDA application: NDA050629

## Active ingredients

- DOXORUBICIN HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0069-4031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-4031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d31d7f58-66d0-4826-b6b5-5914c031965f