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Amiodarone Hydrochloride

NDC 50268-097 · AvPAK

Generic nameAmiodarone Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)AMIODARONE HYDROCHLORIDE
Strength100 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

50268-097-15 — 50 BLISTER PACK in 1 BOX (50268-097-15) / 1 TABLET in 1 BLISTER PACK (50268-097-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8258 — Amiodarone Hydrochloride, 0615-8607 — Amiodarone Hydrochloride, 0904-6993 — Amiodarone Hydrochloride, 0904-7576 — Amiodarone Hydrochloride, 29300-359 — Amiodarone Hydrochloride, 43066-150 — amiodarone hydrochloride, 43066-360 — amiodarone hydrochloride, 48433-154 — amiodarone hydrochloride, 50090-3015 — Amiodarone Hydrochloride, 50090-5766 — 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, 51672-4057 — Amiodarone Hydrochloride, 55150-180 — 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.