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Spironolactone - 21695-960-60 - (spironolactone)

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Drug Information of Spironolactone

Product NDC: 21695-960
Proprietary Name: Spironolactone
Non Proprietary Name: spironolactone
Active Ingredient(s): 50    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: 21695-960
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040750
Marketing Category: ANDA
Start Marketing Date: 20060829

Package Information of Spironolactone

Package NDC: 21695-960-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21695-960-60)

NDC Information of Spironolactone

NDC Code 21695-960-60
Proprietary Name Spironolactone
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21695-960-60)
Product NDC 21695-960
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060829
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name SPIRONOLACTONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information