Atenolol - 50742-101-10 - (atenolol)

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Drug Information of Atenolol

Product NDC: 50742-101
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: 50742-101
Labeler Name: Ingenus Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20110130

Package Information of Atenolol

Package NDC: 50742-101-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (50742-101-10)

NDC Information of Atenolol

NDC Code 50742-101-10
Proprietary Name Atenolol
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (50742-101-10)
Product NDC 50742-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110130
Marketing Category Name ANDA
Labeler Name Ingenus Pharmaceuticals, LLC
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