NDC 82804-215 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-215

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208045
Marketed since
March 10, 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
82804-215-3030 TABLET in 1 BOTTLE (82804-215-30)Mar 31, 2025

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