NDC 16729-349 – lurasidone hydrochloride

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

Human Prescription Drug

Product NDC16729-349

Product details

Brand name
lurasidone hydrochloride
Generic name
lurasidone hydrochloride
Labeler
Accord Healthcare, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208049
Marketed since
February 20, 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
16729-349-1030 TABLET, FILM COATED in 1 BOTTLE (16729-349-10)Feb 20, 2023

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