NDC 72205-208 – Lurasidone hydrochloride

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

Human Prescription Drug

Product NDC72205-208

Product details

Brand name
Lurasidone hydrochloride
Generic name
Lurasidone hydrochloride
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208037
Marketed since
February 9, 2023
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
72205-208-05500 TABLET, FILM COATED in 1 BOTTLE (72205-208-05)Feb 20, 2023
72205-208-3030 TABLET, FILM COATED in 1 BOTTLE (72205-208-30)Feb 20, 2023
72205-208-9090 TABLET, FILM COATED in 1 BOTTLE (72205-208-90)Feb 20, 2023

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