Digoxin - 55154-5254-9 - (DIGOXIN)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 55154-5254
Proprietary Name: Digoxin
Non Proprietary Name: DIGOXIN
Active Ingredient(s): 125    ug/1 & nbsp;   DIGOXIN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Digoxin

Product NDC: 55154-5254
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078556
Marketing Category: ANDA
Start Marketing Date: 20091201

Package Information of Digoxin

Package NDC: 55154-5254-9
Package Description: 30 TABLET in 1 BLISTER PACK (55154-5254-9)

NDC Information of Digoxin

NDC Code 55154-5254-9
Proprietary Name Digoxin
Package Description 30 TABLET in 1 BLISTER PACK (55154-5254-9)
Product NDC 55154-5254
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIGOXIN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name DIGOXIN
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of Digoxin


General Information