Atenolol - 63629-1740-1 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 63629-1740
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 50    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 63629-1740
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20071204

Package Information of Atenolol

Package NDC: 63629-1740-1
Package Description: 30 TABLET in 1 BOTTLE (63629-1740-1)

NDC Information of Atenolol

NDC Code 63629-1740-1
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BOTTLE (63629-1740-1)
Product NDC 63629-1740
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071204
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ATENOLOL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information