Atenolol - 53489-536-10 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 53489-536
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 25    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 53489-536
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074499
Marketing Category: ANDA
Start Marketing Date: 19970730

Package Information of Atenolol

Package NDC: 53489-536-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (53489-536-10)

NDC Information of Atenolol

NDC Code 53489-536-10
Proprietary Name Atenolol
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (53489-536-10)
Product NDC 53489-536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970730
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name ATENOLOL
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information