Home > National Drug Code (NDC) > Atenolol and Chlorthalidone

Atenolol and Chlorthalidone - 54868-3064-1 - (Atenolol and Chlorthalidone)

Alphabetical Index


Drug Information of Atenolol and Chlorthalidone

Product NDC: 54868-3064
Proprietary Name: Atenolol and Chlorthalidone
Non Proprietary Name: Atenolol and Chlorthalidone
Active Ingredient(s): 100; 25    mg/1; mg/1 & nbsp;   Atenolol and Chlorthalidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol and Chlorthalidone

Product NDC: 54868-3064
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073665
Marketing Category: ANDA
Start Marketing Date: 20050505

Package Information of Atenolol and Chlorthalidone

Package NDC: 54868-3064-1
Package Description: 90 TABLET in 1 BOTTLE (54868-3064-1)

NDC Information of Atenolol and Chlorthalidone

NDC Code 54868-3064-1
Proprietary Name Atenolol and Chlorthalidone
Package Description 90 TABLET in 1 BOTTLE (54868-3064-1)
Product NDC 54868-3064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol and Chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050505
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ATENOLOL; CHLORTHALIDONE
Strength Number 100; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Atenolol and Chlorthalidone


General Information