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Lurasidone hydrochloride

NDC 70518-4241 · REMEDYREPACK INC.

Generic nameLurasidone hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

70518-4241-0 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4241-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68382-965 — Lurasidone hydrochloride, 68382-966 — Lurasidone hydrochloride, 68382-967 — Lurasidone hydrochloride, 68382-968 — Lurasidone hydrochloride, 69097-937 — Lurasidone Hydrochloride, 69097-938 — Lurasidone Hydrochloride, 69097-939 — Lurasidone Hydrochloride, 69097-941 — Lurasidone Hydrochloride, 69097-942 — Lurasidone Hydrochloride, 70518-4117 — Lurasidone hydrochloride, 70518-4260 — lurasidone hydrochloride, 70518-4427 — lurasidone hydrochloride, 70518-4491 — Lurasidone Hydrochloride, 70518-4563 — Lurasidone Hydrochloride, 70771-1734 — Lurasidone hydrochloride, 70771-1735 — Lurasidone hydrochloride, 70771-1736 — Lurasidone hydrochloride, 70771-1737 — Lurasidone hydrochloride, 70771-1738 — Lurasidone hydrochloride, 72189-598 — Lurasidone HCL, +117 more

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