Atenolol - 54868-1971-0 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 54868-1971
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: 54868-1971
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 19990304

Package Information of Atenolol

Package NDC: 54868-1971-0
Package Description: 60 TABLET in 1 BOTTLE (54868-1971-0)

NDC Information of Atenolol

NDC Code 54868-1971-0
Proprietary Name Atenolol
Package Description 60 TABLET in 1 BOTTLE (54868-1971-0)
Product NDC 54868-1971
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990304
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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