NDC 53746-082 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 60 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC53746-082

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208002
Marketed since
July 5, 2024
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
53746-082-3030 TABLET, COATED in 1 BOTTLE (53746-082-30)Jul 5, 2024

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