Lurasidone Hydrochloride 00904-7355-04

Package NDC

00904-7355-04

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 4, 2023
Listing Expires: December 31, 2026
Application: ANDA212244

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Active Ingredients

Ingredient	Strength
Lurasidone Hydrochloride	20 mg/1

Drug Class

Atypical Antipsychotic [EPC]

Selected Package

00904-7355-04Selected

30 BLISTER PACK in 1 CARTON (0904-7355-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK