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Lurasidone Hydrochloride

NDC 47335-639 · Sun Pharmaceutical Industries, Inc.

Generic nameLurasidone Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

47335-639-13 — 500 TABLET in 1 BOTTLE (47335-639-13)

47335-639-81 — 90 TABLET in 1 BOTTLE (47335-639-81)

47335-639-83 — 30 TABLET in 1 BOTTLE (47335-639-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-353 — Lurasidone hydrochloride, 43598-354 — Lurasidone hydrochloride, 43598-355 — Lurasidone Hydrochloride, 46708-494 — Lurasidone Hydrochloride, 46708-495 — Lurasidone Hydrochloride, 46708-496 — Lurasidone Hydrochloride, 46708-497 — Lurasidone Hydrochloride, 46708-498 — Lurasidone Hydrochloride, 47335-578 — Lurasidone Hydrochloride, 47335-579 — Lurasidone Hydrochloride, 47335-684 — Lurasidone Hydrochloride, 47335-685 — Lurasidone Hydrochloride, 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, +117 more

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