Nadolol - 54868-3257-2 - (nadolol)

Alphabetical Index


Drug Information of Nadolol

Product NDC: 54868-3257
Proprietary Name: Nadolol
Non Proprietary Name: nadolol
Active Ingredient(s): 40    mg/1 & nbsp;   nadolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nadolol

Product NDC: 54868-3257
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074172
Marketing Category: ANDA
Start Marketing Date: 20100114

Package Information of Nadolol

Package NDC: 54868-3257-2
Package Description: 30 TABLET in 1 BOTTLE (54868-3257-2)

NDC Information of Nadolol

NDC Code 54868-3257-2
Proprietary Name Nadolol
Package Description 30 TABLET in 1 BOTTLE (54868-3257-2)
Product NDC 54868-3257
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nadolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100114
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name NADOLOL
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Nadolol


General Information