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Atenolol and Chlorthalidone - 53489-532-03 - (Atenolol and Chlorthalidone)

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Drug Information of Atenolol and Chlorthalidone

Product NDC: 53489-532
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: 53489-532
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073582
Marketing Category: ANDA
Start Marketing Date: 19930429

Package Information of Atenolol and Chlorthalidone

Package NDC: 53489-532-03
Package Description: 250 TABLET in 1 BOTTLE, PLASTIC (53489-532-03)

NDC Information of Atenolol and Chlorthalidone

NDC Code 53489-532-03
Proprietary Name Atenolol and Chlorthalidone
Package Description 250 TABLET in 1 BOTTLE, PLASTIC (53489-532-03)
Product NDC 53489-532
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol and Chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930429
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, 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


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