Digoxin - 50564-544-10 - (Digoxin)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 50564-544
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: 50564-544
Labeler Name: Jerome Stevens Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076268
Marketing Category: ANDA
Start Marketing Date: 20020726

Package Information of Digoxin

Package NDC: 50564-544-10
Package Description: 1000 TABLET in 1 BOTTLE (50564-544-10)

NDC Information of Digoxin

NDC Code 50564-544-10
Proprietary Name Digoxin
Package Description 1000 TABLET in 1 BOTTLE (50564-544-10)
Product NDC 50564-544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020726
Marketing Category Name ANDA
Labeler Name Jerome Stevens Pharmaceuticals, Inc.
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