Inspra - 0025-1710-02 - (EPLERENONE)

Alphabetical Index


Drug Information of Inspra

Product NDC: 0025-1710
Proprietary Name: Inspra
Non Proprietary Name: EPLERENONE
Active Ingredient(s): 25    mg/1 & nbsp;   EPLERENONE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Inspra

Product NDC: 0025-1710
Labeler Name: G.D. Searle LLC Division of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021437
Marketing Category: NDA
Start Marketing Date: 20020927

Package Information of Inspra

Package NDC: 0025-1710-02
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0025-1710-02)

NDC Information of Inspra

NDC Code 0025-1710-02
Proprietary Name Inspra
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0025-1710-02)
Product NDC 0025-1710
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
Labeler Name G.D. Searle LLC Division of Pfizer Inc
Substance Name EPLERENONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Inspra


General Information