NDC 46708-494 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-494

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213248
Marketed since
January 24, 2023
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
46708-494-10100 BLISTER PACK in 1 CARTON (46708-494-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 24, 2023
46708-494-3030 TABLET, FILM COATED in 1 BOTTLE (46708-494-30)Jan 24, 2023
46708-494-71500 TABLET, FILM COATED in 1 BOTTLE (46708-494-71)Jan 24, 2023
46708-494-9090 TABLET, FILM COATED in 1 BOTTLE (46708-494-90)Jan 24, 2023
46708-494-911000 TABLET, FILM COATED in 1 BOTTLE (46708-494-91)Jan 24, 2023

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