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amiodarone hydrochloride

NDC 68382-297 · Zydus Pharmaceuticals USA Inc.

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 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Marketing categoryANDA

Packages

68382-297-06 — 30 TABLET in 1 BOTTLE (68382-297-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65219-643 — AMIODARONE HYDROCHLORIDE, 65219-645 — AMIODARONE HYDROCHLORIDE, 65841-631 — Amiodarone hydrochloride, 65841-840 — Amiodarone hydrochloride, 65841-841 — Amiodarone hydrochloride, 65862-732 — Amiodarone Hydrochloride, 67296-2296 — Amiodarone Hydrochloride, 67457-153 — amiodarone hydrochloride, 68083-112 — Amiodarone hydrochloride, 68382-227 — amiodarone hydrochloride, 68382-298 — amiodarone hydrochloride, 70436-232 — amiodarone hydrochloride, 70518-1231 — Amiodarone Hydrochloride, 70518-1939 — Amiodarone Hydrochloride, 70518-3246 — Amiodarone Hydrochloride, 70518-3439 — Amiodarone Hydrochloride, 71335-0881 — Amiodarone Hydrochloride, 71335-1942 — Amiodarone Hydrochloride, 71335-1985 — Amiodarone Hydrochloride, 71610-787 — 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.