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NEXTERONE (AMIODARONE HCI)

NDC 51662-1480 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameNEXTERONE (AMIODARONE HCI)
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)AMIODARONE HYDROCHLORIDE
Strength1.5 mg/mL
Pharmacologic classAntiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Marketing categoryNDA

Packages

51662-1480-1 — 1 BAG in 1 CARTON (51662-1480-1) / 100 mL in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-359 — Amiodarone Hydrochloride, 43066-150 — amiodarone hydrochloride, 43066-360 — amiodarone hydrochloride, 48433-154 — amiodarone hydrochloride, 50090-3015 — Amiodarone Hydrochloride, 50090-5766 — Amiodarone Hydrochloride, 50268-097 — Amiodarone Hydrochloride, 51662-1205 — AMIODARONE HYDROCHLORIDE, 51662-1358 — AMIODARONE HYDROCHLORIDE, 51662-1363 — AMIODARONE HCI, 51662-1481 — NEXTERONE (AMIODARONE HCI), 51672-4025 — Amiodarone Hydrochloride, 51672-4055 — Amiodarone Hydrochloride, 51672-4056 — Amiodarone Hydrochloride, 51672-4057 — Amiodarone Hydrochloride, 55150-180 — Amiodarone Hydrochloride, 55150-181 — Amiodarone Hydrochloride, 55150-182 — Amiodarone Hydrochloride, 55154-3365 — Amiodarone Hydrochloride, 55154-8185 — Amiodarone Hydrochloride, +51 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.