Digoxin - 55289-002-01 - (Digoxin)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 55289-002
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: 55289-002
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076268
Marketing Category: ANDA
Start Marketing Date: 20020726

Package Information of Digoxin

Package NDC: 55289-002-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (55289-002-01)

NDC Information of Digoxin

NDC Code 55289-002-01
Proprietary Name Digoxin
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (55289-002-01)
Product NDC 55289-002
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 PD-Rx 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