NDC 68382-968 – Lurasidone hydrochloride

Lurasidone Hydrochloride 120 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68382-968

Product details

Brand name
Lurasidone hydrochloride
Generic name
Lurasidone hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208052
Marketed since
February 1, 2023
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
68382-968-01100 TABLET, COATED in 1 BOTTLE (68382-968-01)Feb 1, 2023
68382-968-05500 TABLET, COATED in 1 BOTTLE (68382-968-05)Feb 1, 2023
68382-968-0630 TABLET, COATED in 1 BOTTLE (68382-968-06)Feb 1, 2023
68382-968-1690 TABLET, COATED in 1 BOTTLE (68382-968-16)Feb 1, 2023
68382-968-77100 BLISTER PACK in 1 CARTON (68382-968-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-968-30)Feb 1, 2023

Other Lurasidone hydrochloride products