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Spironolactone - 21695-766-30 - (spironolactone)

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Drug Information of Spironolactone

Product NDC: 21695-766
Proprietary Name: Spironolactone
Non Proprietary Name: spironolactone
Active Ingredient(s): 25    mg/1 & nbsp;   spironolactone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone

Product NDC: 21695-766
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089424
Marketing Category: ANDA
Start Marketing Date: 19860723

Package Information of Spironolactone

Package NDC: 21695-766-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (21695-766-30)

NDC Information of Spironolactone

NDC Code 21695-766-30
Proprietary Name Spironolactone
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (21695-766-30)
Product NDC 21695-766
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19860723
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name SPIRONOLACTONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


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