Atenolol - 65841-022-01 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 65841-022
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 25    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 65841-022
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076900
Marketing Category: ANDA
Start Marketing Date: 20050810

Package Information of Atenolol

Package NDC: 65841-022-01
Package Description: 100 TABLET in 1 BOTTLE (65841-022-01)

NDC Information of Atenolol

NDC Code 65841-022-01
Proprietary Name Atenolol
Package Description 100 TABLET in 1 BOTTLE (65841-022-01)
Product NDC 65841-022
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050810
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
Substance Name ATENOLOL
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information