NDC 67877-638 – Lurasidone hydrochloride

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

Human Prescription Drug

Product NDC67877-638

Product details

Brand name
Lurasidone hydrochloride
Generic name
Lurasidone hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212244
Marketed since
January 4, 2023
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
67877-638-05500 TABLET, FILM COATED in 1 BOTTLE (67877-638-05)Jan 4, 2023
67877-638-3030 TABLET, FILM COATED in 1 BOTTLE (67877-638-30)Jan 4, 2023
67877-638-3810 BLISTER PACK in 1 CARTON (67877-638-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-638-33)Jan 4, 2023
67877-638-9090 TABLET, FILM COATED in 1 BOTTLE (67877-638-90)Jan 4, 2023

Other Lurasidone hydrochloride products