NDC 0904-7356 – Lurasidone hydrochloride

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

Human Prescription Drug

Product NDC0904-7356

Product details

Brand name
Lurasidone hydrochloride
Generic name
Lurasidone hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212244
Marketed since
January 4, 2023
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
0904-7356-61100 BLISTER PACK in 1 CARTON (0904-7356-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKFeb 20, 2023

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