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Spironolactone and Hydrochlorothiazide - 53489-144-10 - (Spironolactone and Hydrochlorothiazide)

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Drug Information of Spironolactone and Hydrochlorothiazide

Product NDC: 53489-144
Proprietary Name: Spironolactone and Hydrochlorothiazide
Non Proprietary Name: Spironolactone and Hydrochlorothiazide
Active Ingredient(s): 25; 25    mg/1; mg/1 & nbsp;   Spironolactone and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone and Hydrochlorothiazide

Product NDC: 53489-144
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089534
Marketing Category: ANDA
Start Marketing Date: 19870702

Package Information of Spironolactone and Hydrochlorothiazide

Package NDC: 53489-144-10
Package Description: 1000 TABLET in 1 BOTTLE (53489-144-10)

NDC Information of Spironolactone and Hydrochlorothiazide

NDC Code 53489-144-10
Proprietary Name Spironolactone and Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (53489-144-10)
Product NDC 53489-144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870702
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
Strength Number 25; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Spironolactone and Hydrochlorothiazide


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