United States · FDA National Drug Code directory
NEXTERONE (AMIODARONE HCI)
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51662-1480_11c3bf02-6616-9353-e063-6394a90af9cd
- Product NDC
- 51662-1480
- Form
- INJECTION, SOLUTION
- Composition / generic term
- NEXTERONE (AMIODARONE HCI)
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- NDA
- Marketing start / end (source format)
- 20200129
- Source listing expiry
- 20261231
Source-listed ingredients
- AMIODARONE HYDROCHLORIDE — 1.5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BAG in 1 CARTON (51662-1480-1) / 100 mL in 1 BAG · 51662-1480-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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