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

Atenolol and Chlorthalidone - 0378-2063-01 - (atenolol and chlorthalidone)

Alphabetical Index


Drug Information of Atenolol and Chlorthalidone

Product NDC: 0378-2063
Proprietary Name: Atenolol and Chlorthalidone
Non Proprietary Name: atenolol and chlorthalidone
Active Ingredient(s): 50; 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: 0378-2063
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074203
Marketing Category: ANDA
Start Marketing Date: 20130328

Package Information of Atenolol and Chlorthalidone

Package NDC: 0378-2063-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-2063-01)

NDC Information of Atenolol and Chlorthalidone

NDC Code 0378-2063-01
Proprietary Name Atenolol and Chlorthalidone
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-2063-01)
Product NDC 0378-2063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atenolol and chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130328
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ATENOLOL; CHLORTHALIDONE
Strength Number 50; 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