NDC 23155-891 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 120 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC23155-891

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208058
Marketed since
October 19, 2023
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Lurasidone hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
23155-891-01100 TABLET, FILM COATED in 1 BOTTLE (23155-891-01)Aug 20, 2025
23155-891-0330 TABLET, FILM COATED in 1 BOTTLE (23155-891-03)Aug 20, 2025
23155-891-05500 TABLET, FILM COATED in 1 BOTTLE (23155-891-05)Aug 20, 2025
23155-891-101000 TABLET, FILM COATED in 1 BOTTLE (23155-891-10)Aug 20, 2025
23155-891-1820000 TABLET, FILM COATED in 1 CONTAINER (23155-891-18)Oct 19, 2023

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