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lurasidone hydrochloride

NDC 16729-350 · Accord Healthcare, Inc.

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

Packages

16729-350-10 — 30 TABLET, FILM COATED in 1 BOTTLE (16729-350-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13668-464 — Lurasidone Hydrochloride, 13668-465 — Lurasidone Hydrochloride, 13668-466 — Lurasidone Hydrochloride, 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, 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, 31722-084 — 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.