NDC 13668-737 – Lurasidone Hydrochloride

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

Human Prescription Drug

Product NDC13668-737

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Torrent Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208055
Marketed since
March 2, 2026
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
13668-737-3030 TABLET, FILM COATED in 1 BOTTLE (13668-737-30)Mar 2, 2026
13668-737-9090 TABLET, FILM COATED in 1 BOTTLE (13668-737-90)Mar 2, 2026

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