Atenolol - 51138-098-30 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 51138-098
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 100    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 51138-098
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078512
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Atenolol

Package NDC: 51138-098-30
Package Description: 30 TABLET in 1 BOTTLE (51138-098-30)

NDC Information of Atenolol

NDC Code 51138-098-30
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BOTTLE (51138-098-30)
Product NDC 51138-098
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
Substance Name ATENOLOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information