Bystolic - 54868-5944-0 - (nebivolol hydrochloride)

Alphabetical Index


Drug Information of Bystolic

Product NDC: 54868-5944
Proprietary Name: Bystolic
Non Proprietary Name: nebivolol hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   nebivolol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bystolic

Product NDC: 54868-5944
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021742
Marketing Category: NDA
Start Marketing Date: 20081002

Package Information of Bystolic

Package NDC: 54868-5944-0
Package Description: 30 TABLET in 1 BOTTLE (54868-5944-0)

NDC Information of Bystolic

NDC Code 54868-5944-0
Proprietary Name Bystolic
Package Description 30 TABLET in 1 BOTTLE (54868-5944-0)
Product NDC 54868-5944
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nebivolol hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081002
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name NEBIVOLOL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bystolic


General Information