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lurasidone hydrochloride

NDC 50090-6438 · A-S Medication Solutions

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

Packages

50090-6438-0 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-6438-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 47335-639 — Lurasidone Hydrochloride, 47335-684 — Lurasidone Hydrochloride, 47335-685 — 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, 53746-082 — Lurasidone Hydrochloride, 53746-879 — Lurasidone Hydrochloride, 53746-880 — 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.