NDC 47335-578 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC47335-578

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208066
Marketed since
February 20, 2023
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
47335-578-13500 TABLET in 1 BOTTLE (47335-578-13)Feb 20, 2023
47335-578-8190 TABLET in 1 BOTTLE (47335-578-81)Feb 20, 2023
47335-578-8330 TABLET in 1 BOTTLE (47335-578-83)Feb 20, 2023

Recalls mentioning this NDC

Other Lurasidone hydrochloride products