# Amiodarone Hydrochloride

NDC: 70518-1231
Generic name: Amiodarone Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180530

FDA application: ANDA077234

## 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:"70518-1231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9151c1b-b70c-477b-868a-fffdc5c51830