VIIBRYD - 0456-1120-30 - (vilazodone hydrochloride)

Alphabetical Index


Drug Information of VIIBRYD

Product NDC: 0456-1120
Proprietary Name: VIIBRYD
Non Proprietary Name: vilazodone hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   vilazodone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of VIIBRYD

Product NDC: 0456-1120
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022567
Marketing Category: NDA
Start Marketing Date: 20110429

Package Information of VIIBRYD

Package NDC: 0456-1120-30
Package Description: 30 TABLET in 1 BOTTLE (0456-1120-30)

NDC Information of VIIBRYD

NDC Code 0456-1120-30
Proprietary Name VIIBRYD
Package Description 30 TABLET in 1 BOTTLE (0456-1120-30)
Product NDC 0456-1120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name vilazodone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110429
Marketing Category Name NDA
Labeler Name Forest Laboratories, Inc.
Substance Name VILAZODONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of VIIBRYD


General Information