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Lurasidone hydrochloride

NDC 68382-859 · Zydus Pharmaceuticals USA Inc.

Generic nameLurasidone hydrochloride
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

68382-859-01 — 100 TABLET, COATED in 1 BOTTLE (68382-859-01)

68382-859-05 — 500 TABLET, COATED in 1 BOTTLE (68382-859-05)

68382-859-06 — 30 TABLET, COATED in 1 BOTTLE (68382-859-06)

68382-859-16 — 90 TABLET, COATED in 1 BOTTLE (68382-859-16)

68382-859-77 — 100 BLISTER PACK in 1 CARTON (68382-859-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-859-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67877-638 — lurasidone hydrochloride, 67877-639 — lurasidone hydrochloride, 67877-640 — lurasidone hydrochloride, 67877-641 — lurasidone hydrochloride, 67877-642 — lurasidone hydrochloride, 68180-670 — lurasidone hydrochloride, 68180-671 — lurasidone hydrochloride, 68180-672 — lurasidone hydrochloride, 68180-673 — lurasidone hydrochloride, 68180-674 — lurasidone hydrochloride, 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, +117 more

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