NDC 76282-524 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC76282-524

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208028
Marketed since
February 20, 2023
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
76282-524-3030 TABLET, FILM COATED in 1 BOTTLE (76282-524-30)Feb 20, 2023

Other Lurasidone hydrochloride products