Skip to main content

Lurasidone Hydrochloride

NDC 23155-889 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

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

Packages

23155-889-03 — 30 TABLET, FILM COATED in 1 BOTTLE (23155-889-03)

23155-889-05 — 500 TABLET, FILM COATED in 1 BOTTLE (23155-889-05)

23155-889-09 — 90 TABLET, FILM COATED in 1 BOTTLE (23155-889-09)

23155-889-18 — 40000 TABLET, FILM COATED in 1 CONTAINER (23155-889-18)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13668-467 — Lurasidone Hydrochloride, 13668-509 — Lurasidone hydrochloride, 13668-737 — Lurasidone Hydrochloride, 16729-346 — lurasidone hydrochloride, 16729-347 — lurasidone hydrochloride, 16729-348 — lurasidone hydrochloride, 16729-349 — lurasidone hydrochloride, 16729-350 — lurasidone hydrochloride, 23155-887 — Lurasidone Hydrochloride, 23155-888 — 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, 31722-084 — Lurasidone Hydrochloride, 33342-419 — lurasidone hydrochloride, 33342-420 — lurasidone hydrochloride, 33342-421 — 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.