NDC 67046-1659 – Lurasidone Hydrochloride

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

Human Prescription Drug

Product NDC67046-1659

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213248
Marketed since
February 12, 2026
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
67046-1659-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1659-3)Feb 12, 2026

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