Atenolol - 51079-684-20 - (atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 51079-684
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: 51079-684
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073457
Marketing Category: ANDA
Start Marketing Date: 20130321

Package Information of Atenolol

Package NDC: 51079-684-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-684-20) > 1 TABLET in 1 BLISTER PACK (51079-684-01)

NDC Information of Atenolol

NDC Code 51079-684-20
Proprietary Name Atenolol
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-684-20) > 1 TABLET in 1 BLISTER PACK (51079-684-01)
Product NDC 51079-684
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130321
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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