TENORETIC - 0310-0115-10 - (Atenolol and Chlorthalidone)

Alphabetical Index


Drug Information of TENORETIC

Product NDC: 0310-0115
Proprietary Name: TENORETIC
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 TENORETIC

Product NDC: 0310-0115
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018760
Marketing Category: NDA
Start Marketing Date: 19900901

Package Information of TENORETIC

Package NDC: 0310-0115-10
Package Description: 100 TABLET in 1 BOTTLE (0310-0115-10)

NDC Information of TENORETIC

NDC Code 0310-0115-10
Proprietary Name TENORETIC
Package Description 100 TABLET in 1 BOTTLE (0310-0115-10)
Product NDC 0310-0115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol and Chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900901
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
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 TENORETIC


General Information