NDC 65162-879 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC65162-879

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208002
Marketed since
January 2, 2023
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65162-879-0330 TABLET, COATED in 1 BOTTLE (65162-879-03)Jan 2, 2023
65162-879-0990 TABLET, COATED in 1 BOTTLE (65162-879-09)Jan 2, 2023
65162-879-50500 TABLET, COATED in 1 BOTTLE (65162-879-50)Jan 2, 2023

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