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Spironolactone - 65162-511-09 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 65162-511
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: 65162-511
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091426
Marketing Category: ANDA
Start Marketing Date: 20100802

Package Information of Spironolactone

Package NDC: 65162-511-09
Package Description: 90 TABLET in 1 BOTTLE (65162-511-09)

NDC Information of Spironolactone

NDC Code 65162-511-09
Proprietary Name Spironolactone
Package Description 90 TABLET in 1 BOTTLE (65162-511-09)
Product NDC 65162-511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100802
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
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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