# NEXTERONE (AMIODARONE HCI)

NDC: 51662-1480
Generic name: NEXTERONE (AMIODARONE HCI)
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200129

FDA application: NDA022325

## Active ingredients

- AMIODARONE HYDROCHLORIDE: 1.5 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1480"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1480
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9d4d66f7-fa14-e832-e053-2a95a90a8b62