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lurasidone hydrochloride

NDC 67877-641 · Ascend Laboratories, LLC

Generic namelurasidone hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength80 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

67877-641-05 — 500 TABLET, FILM COATED in 1 BOTTLE (67877-641-05)

67877-641-30 — 30 TABLET, FILM COATED in 1 BOTTLE (67877-641-30)

67877-641-38 — 10 BLISTER PACK in 1 CARTON (67877-641-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-641-33)

67877-641-90 — 90 TABLET, FILM COATED in 1 BOTTLE (67877-641-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-954 — LURASIDONE HYDROCHLORIDE, 65862-955 — LURASIDONE HYDROCHLORIDE, 65862-956 — LURASIDONE HYDROCHLORIDE, 65862-957 — LURASIDONE HYDROCHLORIDE, 67046-1637 — Lurasidone Hydrochloride, 67046-1654 — LURASIDONE HYDROCHLORIDE, 67046-1659 — Lurasidone Hydrochloride, 67877-638 — lurasidone hydrochloride, 67877-639 — lurasidone hydrochloride, 67877-640 — lurasidone hydrochloride, 67877-642 — lurasidone hydrochloride, 68180-670 — lurasidone hydrochloride, 68180-671 — lurasidone hydrochloride, 68180-672 — lurasidone hydrochloride, 68180-673 — lurasidone hydrochloride, 68180-674 — lurasidone hydrochloride, 68382-859 — Lurasidone hydrochloride, 68382-965 — Lurasidone hydrochloride, 68382-966 — Lurasidone hydrochloride, 68382-967 — 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.