NDC 51407-833 – Lurasidone Hydrochloride

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

Human Prescription Drug

Product NDC51407-833

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208058
Marketed since
September 4, 2019
Marketing end
September 30, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
51407-833-05500 TABLET, FILM COATED in 1 BOTTLE (51407-833-05)Oct 23, 2023

Other Lurasidone hydrochloride products