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Spironolactone - 53489-329-07 - (spironolactone)

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Drug Information of Spironolactone

Product NDC: 53489-329
Proprietary Name: Spironolactone
Non Proprietary Name: spironolactone
Active Ingredient(s): 100    mg/1 & nbsp;   spironolactone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone

Product NDC: 53489-329
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089424
Marketing Category: ANDA
Start Marketing Date: 19860723

Package Information of Spironolactone

Package NDC: 53489-329-07
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-07)

NDC Information of Spironolactone

NDC Code 53489-329-07
Proprietary Name Spironolactone
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-07)
Product NDC 53489-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19860723
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name SPIRONOLACTONE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information