# doxorubicin hydrochloride

NDC: 62332-810
Generic name: doxorubicin hydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SUSPENSION, LIPOSOMAL
Routes: INTRAVENOUS
Marketing started: 20250627

FDA application: ANDA219199

## 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:"62332-810"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-810
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9cb8a8d-944f-4fe1-bfba-c55904a79fda