Atenolol - 55154-5056-0 - (atenolol)

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Drug Information of Atenolol

Product NDC: 55154-5056
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: 55154-5056
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073457
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Atenolol

Package NDC: 55154-5056-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5056-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Atenolol

NDC Code 55154-5056-0
Proprietary Name Atenolol
Package Description 10 BLISTER PACK in 1 BAG (55154-5056-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5056
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name Cardinal Health
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