NDC 63402-306 – Latuda

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

Human Prescription Drug

Product NDC63402-306

Product details

Brand name
Latuda
Generic name
Lurasidone hydrochloride
Labeler
Sumitomo Pharma America, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA200603
Marketed since
July 12, 2013
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Latuda →

Package NDC codes (5)

Package NDCDescriptionSince
63402-306-044 BLISTER PACK in 1 CARTON (63402-306-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-306-07)Jul 12, 2013
63402-306-1010 BLISTER PACK in 1 CARTON (63402-306-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-306-01)Jul 12, 2013
63402-306-3030 TABLET, FILM COATED in 1 BOTTLE (63402-306-30)Jul 12, 2013
63402-306-50500 TABLET, FILM COATED in 1 BOTTLE (63402-306-50)Jul 12, 2013
63402-306-9090 TABLET, FILM COATED in 1 BOTTLE (63402-306-90)Jul 12, 2013

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