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Lurasidone Hydrochloride

NDC 65162-879 · Amneal Pharmaceuticals LLC

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

Packages

65162-879-03 — 30 TABLET, COATED in 1 BOTTLE (65162-879-03)

65162-879-09 — 90 TABLET, COATED in 1 BOTTLE (65162-879-09)

65162-879-50 — 500 TABLET, COATED in 1 BOTTLE (65162-879-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-495 — Lurasidone Hydrochloride, 62332-496 — Lurasidone Hydrochloride, 62332-497 — Lurasidone Hydrochloride, 62332-498 — Lurasidone Hydrochloride, 63402-302 — lurasidone hydrochloride, 63402-304 — lurasidone hydrochloride, 63402-306 — lurasidone hydrochloride, 63402-308 — lurasidone hydrochloride, 63402-312 — lurasidone hydrochloride, 65162-082 — Lurasidone Hydrochloride, 65162-880 — Lurasidone Hydrochloride, 65162-881 — Lurasidone Hydrochloride, 65162-882 — Lurasidone Hydrochloride, 65862-953 — LURASIDONE HYDROCHLORIDE, 65862-954 — LURASIDONE HYDROCHLORIDE, 65862-955 — LURASIDONE HYDROCHLORIDE, 65862-956 — LURASIDONE HYDROCHLORIDE, 65862-957 — LURASIDONE HYDROCHLORIDE, 67046-1637 — Lurasidone Hydrochloride, 67046-1654 — 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.