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Lurasidone Hydrochloride

NDC 31722-084 · Camber Pharmaceuticals, Inc.

Generic nameLurasidone Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength120 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

31722-084-05 — 500 TABLET, FILM COATED in 1 BOTTLE (31722-084-05)

31722-084-30 — 30 TABLET, FILM COATED in 1 BOTTLE (31722-084-30)

31722-084-90 — 90 TABLET, FILM COATED in 1 BOTTLE (31722-084-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16729-350 — lurasidone hydrochloride, 23155-887 — Lurasidone Hydrochloride, 23155-888 — Lurasidone Hydrochloride, 23155-889 — Lurasidone Hydrochloride, 23155-890 — Lurasidone Hydrochloride, 23155-891 — Lurasidone Hydrochloride, 31722-080 — Lurasidone Hydrochloride, 31722-081 — Lurasidone Hydrochloride, 31722-082 — Lurasidone Hydrochloride, 31722-083 — Lurasidone Hydrochloride, 33342-419 — lurasidone hydrochloride, 33342-420 — lurasidone hydrochloride, 33342-421 — lurasidone hydrochloride, 33342-422 — lurasidone hydrochloride, 33342-423 — lurasidone hydrochloride, 43598-351 — Lurasidone hydrochloride, 43598-352 — Lurasidone hydrochloride, 43598-353 — Lurasidone hydrochloride, 43598-354 — Lurasidone hydrochloride, 43598-355 — 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.