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Spironolactone - 54868-0700-5 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 54868-0700
Proprietary Name: Spironolactone
Non Proprietary Name: Spironolactone
Active Ingredient(s): 25    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: 54868-0700
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040353
Marketing Category: ANDA
Start Marketing Date: 19940325

Package Information of Spironolactone

Package NDC: 54868-0700-5
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (54868-0700-5)

NDC Information of Spironolactone

NDC Code 54868-0700-5
Proprietary Name Spironolactone
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (54868-0700-5)
Product NDC 54868-0700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940325
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name SPIRONOLACTONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information