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Lurasidone Hydrochloride

NDC 76282-522 · Exelan Pharmaceuticals Inc.

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

Packages

76282-522-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76282-522-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70771-1734 — Lurasidone hydrochloride, 70771-1735 — Lurasidone hydrochloride, 70771-1736 — Lurasidone hydrochloride, 70771-1737 — Lurasidone hydrochloride, 70771-1738 — Lurasidone hydrochloride, 72189-598 — Lurasidone HCL, 72205-207 — lurasidone hydrochloride, 72205-208 — lurasidone hydrochloride, 72205-209 — lurasidone hydrochloride, 72205-210 — lurasidone hydrochloride, 72205-211 — lurasidone hydrochloride, 72603-621 — lurasidone hydrochloride, 72603-622 — lurasidone hydrochloride, 72603-623 — lurasidone hydrochloride, 72603-624 — lurasidone hydrochloride, 76282-523 — Lurasidone Hydrochloride, 76282-524 — Lurasidone Hydrochloride, 76282-525 — Lurasidone Hydrochloride, 76282-534 — Lurasidone Hydrochloride, 82804-215 — 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.