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Spironolactone - 0781-1599-10 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 0781-1599
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: 0781-1599
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086809
Marketing Category: ANDA
Start Marketing Date: 19820101

Package Information of Spironolactone

Package NDC: 0781-1599-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1599-10)

NDC Information of Spironolactone

NDC Code 0781-1599-10
Proprietary Name Spironolactone
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1599-10)
Product NDC 0781-1599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19820101
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name SPIRONOLACTONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information