Atenolol - 67296-0671-1 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 67296-0671
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: 67296-0671
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20071204

Package Information of Atenolol

Package NDC: 67296-0671-1
Package Description: 10 TABLET in 1 BOTTLE (67296-0671-1)

NDC Information of Atenolol

NDC Code 67296-0671-1
Proprietary Name Atenolol
Package Description 10 TABLET in 1 BOTTLE (67296-0671-1)
Product NDC 67296-0671
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071204
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
Substance Name ATENOLOL
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


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