NDC 72603-624 – Lurasidone hydrochloride

Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72603-624

Product details

Brand name
Lurasidone hydrochloride
Generic name
Lurasidone hydrochloride
Labeler
NorthStar RxLLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212124
Marketed since
April 8, 2025
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
72603-624-0130 TABLET, FILM COATED in 1 BOTTLE (72603-624-01)Apr 8, 2025

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