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Lurasidone hydrochloride

NDC 43598-351 · Dr. Reddys Laboratories Inc

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

Packages

43598-351-05 — 500 TABLET, FILM COATED in 1 BOTTLE (43598-351-05)

43598-351-30 — 30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)

43598-351-78 — 10 BLISTER PACK in 1 CARTON (43598-351-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-351-79)

43598-351-90 — 90 TABLET, FILM COATED in 1 BOTTLE (43598-351-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-080 — Lurasidone Hydrochloride, 31722-081 — Lurasidone Hydrochloride, 31722-082 — Lurasidone Hydrochloride, 31722-083 — Lurasidone Hydrochloride, 31722-084 — Lurasidone Hydrochloride, 33342-419 — lurasidone hydrochloride, 33342-420 — lurasidone hydrochloride, 33342-421 — lurasidone hydrochloride, 33342-422 — lurasidone hydrochloride, 33342-423 — lurasidone hydrochloride, 43598-352 — Lurasidone hydrochloride, 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, +117 more

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