Atenolol - 65862-168-99 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 65862-168
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: 65862-168
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078512
Marketing Category: ANDA
Start Marketing Date: 20071031

Package Information of Atenolol

Package NDC: 65862-168-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-168-99)

NDC Information of Atenolol

NDC Code 65862-168-99
Proprietary Name Atenolol
Package Description 1000 TABLET in 1 BOTTLE (65862-168-99)
Product NDC 65862-168
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071031
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma 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