NDC 70518-4491 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4491

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA218174
Marketed since
October 4, 2025
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-4491-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4491-0)Oct 4, 2025

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