Eplerenone - 59762-1720-2 - (EPLERENONE)

Alphabetical Index


Drug Information of Eplerenone

Product NDC: 59762-1720
Proprietary Name: Eplerenone
Non Proprietary Name: EPLERENONE
Active Ingredient(s): 50    mg/1 & nbsp;   EPLERENONE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Eplerenone

Product NDC: 59762-1720
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021437
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20020927

Package Information of Eplerenone

Package NDC: 59762-1720-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (59762-1720-2)

NDC Information of Eplerenone

NDC Code 59762-1720-2
Proprietary Name Eplerenone
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (59762-1720-2)
Product NDC 59762-1720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPLERENONE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020927
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name EPLERENONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Eplerenone


General Information