Digoxin - 0904-5921-61 - (Digoxin)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 0904-5921
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: 0904-5921
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077002
Marketing Category: ANDA
Start Marketing Date: 20090610

Package Information of Digoxin

Package NDC: 0904-5921-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5921-61)

NDC Information of Digoxin

NDC Code 0904-5921-61
Proprietary Name Digoxin
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5921-61)
Product NDC 0904-5921
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090610
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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