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Lurasidone Hydrochloride

NDC 51407-832 · Golden State Medical Supply, Inc.

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

Packages

51407-832-05 — 500 TABLET, FILM COATED in 1 BOTTLE (51407-832-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-497 — Lurasidone Hydrochloride, 46708-498 — Lurasidone Hydrochloride, 47335-578 — Lurasidone Hydrochloride, 47335-579 — Lurasidone Hydrochloride, 47335-639 — Lurasidone Hydrochloride, 47335-684 — Lurasidone Hydrochloride, 47335-685 — Lurasidone Hydrochloride, 50090-6438 — lurasidone hydrochloride, 50090-7078 — lurasidone hydrochloride, 50090-7170 — 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, 53746-880 — Lurasidone Hydrochloride, 53746-881 — Lurasidone Hydrochloride, 53746-882 — Lurasidone Hydrochloride, 60687-747 — 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.