Home > National Drug Code (NDC) > Spironolactone

Spironolactone - 0228-2672-50 - (Spironolactone)

Alphabetical Index


Drug Information of Spironolactone

Product NDC: 0228-2672
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: 0228-2672
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040353
Marketing Category: ANDA
Start Marketing Date: 20070103

Package Information of Spironolactone

Package NDC: 0228-2672-50
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0228-2672-50)

NDC Information of Spironolactone

NDC Code 0228-2672-50
Proprietary Name Spironolactone
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0228-2672-50)
Product NDC 0228-2672
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070103
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name SPIRONOLACTONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


General Information