Latuda - 63402-302-04 - (lurasidone hydrochloride)

Alphabetical Index


Drug Information of Latuda

Product NDC: 63402-302
Proprietary Name: Latuda
Non Proprietary Name: lurasidone hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   lurasidone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Latuda

Product NDC: 63402-302
Labeler Name: Sunovion Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA200603
Marketing Category: NDA
Start Marketing Date: 20111207

Package Information of Latuda

Package NDC: 63402-302-04
Package Description: 4 BLISTER PACK in 1 CARTON (63402-302-04) > 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07)

NDC Information of Latuda

NDC Code 63402-302-04
Proprietary Name Latuda
Package Description 4 BLISTER PACK in 1 CARTON (63402-302-04) > 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07)
Product NDC 63402-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lurasidone hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name NDA
Labeler Name Sunovion Pharmaceuticals Inc.
Substance Name LURASIDONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Latuda


General Information