Atenolol - 42291-142-18 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 42291-142
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: 42291-142
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074056
Marketing Category: ANDA
Start Marketing Date: 20130617

Package Information of Atenolol

Package NDC: 42291-142-18
Package Description: 180 TABLET in 1 BOTTLE (42291-142-18)

NDC Information of Atenolol

NDC Code 42291-142-18
Proprietary Name Atenolol
Package Description 180 TABLET in 1 BOTTLE (42291-142-18)
Product NDC 42291-142
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130617
Marketing Category Name ANDA
Labeler Name AvKARE, 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