Atenolol - 16714-033-06 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 16714-033
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: 16714-033
Labeler Name: Northstar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078254
Marketing Category: ANDA
Start Marketing Date: 20091110

Package Information of Atenolol

Package NDC: 16714-033-06
Package Description: 1000 TABLET in 1 BOTTLE (16714-033-06)

NDC Information of Atenolol

NDC Code 16714-033-06
Proprietary Name Atenolol
Package Description 1000 TABLET in 1 BOTTLE (16714-033-06)
Product NDC 16714-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091110
Marketing Category Name ANDA
Labeler Name Northstar RxLLC
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