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Spironolactone - 55154-5065-0 - (spironolactone)

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Drug Information of Spironolactone

Product NDC: 55154-5065
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: 55154-5065
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040424
Marketing Category: ANDA
Start Marketing Date: 20110204

Package Information of Spironolactone

Package NDC: 55154-5065-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5065-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Spironolactone

NDC Code 55154-5065-0
Proprietary Name Spironolactone
Package Description 10 BLISTER PACK in 1 BAG (55154-5065-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5065
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110204
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name SPIRONOLACTONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


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