Atenolol - 53489-530-10 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 53489-530
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 100    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 53489-530
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073476
Marketing Category: ANDA
Start Marketing Date: 19930330

Package Information of Atenolol

Package NDC: 53489-530-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (53489-530-10)

NDC Information of Atenolol

NDC Code 53489-530-10
Proprietary Name Atenolol
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (53489-530-10)
Product NDC 53489-530
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930330
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name ATENOLOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information