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Spironolactone - 0904-5952-06 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 0904-5952
Proprietary Name: Spironolactone
Non Proprietary Name: Spironolactone
Active Ingredient(s): 50    mg/1 & nbsp;   Spironolactone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone

Product NDC: 0904-5952
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040353
Marketing Category: ANDA
Start Marketing Date: 20091102

Package Information of Spironolactone

Package NDC: 0904-5952-06
Package Description: 50 TABLET in 1 BOX, UNIT-DOSE (0904-5952-06)

NDC Information of Spironolactone

NDC Code 0904-5952-06
Proprietary Name Spironolactone
Package Description 50 TABLET in 1 BOX, UNIT-DOSE (0904-5952-06)
Product NDC 0904-5952
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091102
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name SPIRONOLACTONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information