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Atenolol and Chlorthalidone - 0591-5782-01 - (Atenolol and Chlorthalidone)

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Drug Information of Atenolol and Chlorthalidone

Product NDC: 0591-5782
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: 0591-5782
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073665
Marketing Category: ANDA
Start Marketing Date: 19920801

Package Information of Atenolol and Chlorthalidone

Package NDC: 0591-5782-01
Package Description: 100 TABLET in 1 BOTTLE (0591-5782-01)

NDC Information of Atenolol and Chlorthalidone

NDC Code 0591-5782-01
Proprietary Name Atenolol and Chlorthalidone
Package Description 100 TABLET in 1 BOTTLE (0591-5782-01)
Product NDC 0591-5782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol and Chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920801
Marketing Category Name ANDA
Labeler Name Watson Laboratories, 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


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