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Amiodarone Hydrochloride

NDC 51672-4057 · Sun Pharmaceutical Industries, Inc.

Generic nameAmiodarone Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)AMIODARONE HYDROCHLORIDE
Strength400 mg/1
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 categoryANDA

Packages

51672-4057-0 — 10 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK

51672-4057-6 — 30 TABLET in 1 BOTTLE (51672-4057-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-5766 — Amiodarone Hydrochloride, 50268-097 — Amiodarone Hydrochloride, 51662-1205 — AMIODARONE HYDROCHLORIDE, 51662-1358 — AMIODARONE HYDROCHLORIDE, 51662-1363 — AMIODARONE HCI, 51662-1480 — NEXTERONE (AMIODARONE HCI), 51662-1481 — NEXTERONE (AMIODARONE HCI), 51672-4025 — Amiodarone Hydrochloride, 51672-4055 — Amiodarone Hydrochloride, 51672-4056 — Amiodarone Hydrochloride, 55150-180 — Amiodarone Hydrochloride, 55150-181 — Amiodarone Hydrochloride, 55150-182 — Amiodarone Hydrochloride, 55154-3365 — Amiodarone Hydrochloride, 55154-8185 — Amiodarone Hydrochloride, 60687-437 — Amiodarone Hydrochloride, 62135-576 — Amiodarone Hydrochloride, 62135-577 — Amiodarone Hydrochloride, 62135-578 — Amiodarone Hydrochloride, 63323-616 — 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.