# Amiodarone Hydrochloride

NDC: 70436-232
Generic name: amiodarone hydrochloride
Labeler / Manufacturer: Slate Run Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20241031

FDA application: ANDA218253

## 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:"70436-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a53668c-adda-44c2-a743-e79e467437e3