Atenolol - 0781-1507-01 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 0781-1507
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: 0781-1507
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073026
Marketing Category: ANDA
Start Marketing Date: 19910917

Package Information of Atenolol

Package NDC: 0781-1507-01
Package Description: 100 TABLET in 1 BOTTLE (0781-1507-01)

NDC Information of Atenolol

NDC Code 0781-1507-01
Proprietary Name Atenolol
Package Description 100 TABLET in 1 BOTTLE (0781-1507-01)
Product NDC 0781-1507
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19910917
Marketing Category Name ANDA
Labeler Name Sandoz 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