# Amiodarone Hydrochloride

NDC: 65219-643
Generic name: AMIODARONE HYDROCHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250505

FDA application: ANDA075761

## Active ingredients

- AMIODARONE HYDROCHLORIDE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-643"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-643
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9772ab48-2ef1-4b9f-9a27-794f3e7e5c7a