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Latuda

NDC 63402-304 · Sumitomo Pharma America, Inc.

Generic namelurasidone hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryNDA

Packages

63402-304-04 — 4 BLISTER PACK in 1 CARTON (63402-304-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-07)

63402-304-10 — 10 BLISTER PACK in 1 CARTON (63402-304-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-01)

63402-304-30 — 30 TABLET, FILM COATED in 1 BOTTLE (63402-304-30)

63402-304-50 — 500 TABLET, FILM COATED in 1 BOTTLE (63402-304-50)

63402-304-90 — 90 TABLET, FILM COATED in 1 BOTTLE (63402-304-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-747 — Lurasidone Hydrochloride, 60687-758 — Lurasidone Hydrochloride, 60687-769 — Lurasidone Hydrochloride, 60687-780 — Lurasidone Hydrochloride, 62332-494 — Lurasidone Hydrochloride, 62332-495 — Lurasidone Hydrochloride, 62332-496 — Lurasidone Hydrochloride, 62332-497 — Lurasidone Hydrochloride, 62332-498 — Lurasidone Hydrochloride, 63402-302 — lurasidone hydrochloride, 63402-306 — lurasidone hydrochloride, 63402-308 — lurasidone hydrochloride, 63402-312 — lurasidone hydrochloride, 65162-082 — Lurasidone Hydrochloride, 65162-879 — Lurasidone Hydrochloride, 65162-880 — Lurasidone Hydrochloride, 65162-881 — Lurasidone Hydrochloride, 65162-882 — Lurasidone Hydrochloride, 65862-953 — LURASIDONE HYDROCHLORIDE, 65862-954 — 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.