Home > National Drug Code (NDC) > Spironolactone

Spironolactone - 49349-680-02 - (Spironolactone)

Alphabetical Index


Drug Information of Spironolactone

Product NDC: 49349-680
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: 49349-680
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040353
Marketing Category: ANDA
Start Marketing Date: 20110512

Package Information of Spironolactone

Package NDC: 49349-680-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-680-02)

NDC Information of Spironolactone

NDC Code 49349-680-02
Proprietary Name Spironolactone
Package Description 30 TABLET in 1 BLISTER PACK (49349-680-02)
Product NDC 49349-680
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110512
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