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Lurasidone Hydrochloride

NDC 53746-880 · Amneal Pharmaceuticals of New York LLC

Generic nameLurasidone Hydrochloride
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

53746-880-30 — 30 TABLET, COATED in 1 BOTTLE (53746-880-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6438 — lurasidone hydrochloride, 50090-7078 — lurasidone hydrochloride, 50090-7170 — lurasidone hydrochloride, 51407-832 — Lurasidone Hydrochloride, 51407-833 — Lurasidone Hydrochloride, 51407-836 — Lurasidone Hydrochloride, 51407-837 — Lurasidone Hydrochloride, 51407-838 — Lurasidone Hydrochloride, 53746-082 — Lurasidone Hydrochloride, 53746-879 — Lurasidone Hydrochloride, 53746-881 — Lurasidone Hydrochloride, 53746-882 — Lurasidone Hydrochloride, 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, +117 more

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