Atenolol - 55289-228-03 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 55289-228
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 50    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 55289-228
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20071204

Package Information of Atenolol

Package NDC: 55289-228-03
Package Description: 3 TABLET in 1 BOTTLE, PLASTIC (55289-228-03)

NDC Information of Atenolol

NDC Code 55289-228-03
Proprietary Name Atenolol
Package Description 3 TABLET in 1 BOTTLE, PLASTIC (55289-228-03)
Product NDC 55289-228
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 PD-Rx Pharmaceuticals, Inc.
Substance Name ATENOLOL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information