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spironolactone - 59762-5011-2 - (SPIRONOLACTONE)

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Drug Information of spironolactone

Product NDC: 59762-5011
Proprietary Name: spironolactone
Non Proprietary Name: SPIRONOLACTONE
Active Ingredient(s): 25    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: 59762-5011
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012151
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19600121

Package Information of spironolactone

Package NDC: 59762-5011-2
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (59762-5011-2)

NDC Information of spironolactone

NDC Code 59762-5011-2
Proprietary Name spironolactone
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (59762-5011-2)
Product NDC 59762-5011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SPIRONOLACTONE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19600121
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name SPIRONOLACTONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of spironolactone


General Information