Home > National Drug Code (NDC) > Spironolactone

Spironolactone - 52125-603-02 - (spironolactone)

Alphabetical Index


Drug Information of Spironolactone

Product NDC: 52125-603
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: 52125-603
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089424
Marketing Category: ANDA
Start Marketing Date: 20130528

Package Information of Spironolactone

Package NDC: 52125-603-02
Package Description: 30 TABLET in 1 VIAL (52125-603-02)

NDC Information of Spironolactone

NDC Code 52125-603-02
Proprietary Name Spironolactone
Package Description 30 TABLET in 1 VIAL (52125-603-02)
Product NDC 52125-603
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130528
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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