NDC 60687-769 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60687-769

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212244
Marketed since
May 9, 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
60687-769-9420 BLISTER PACK in 1 CARTON (60687-769-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-769-11)May 9, 2023

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