Digoxin - 63629-3870-4 - (Digoxin)

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Drug Information of Digoxin

Product NDC: 63629-3870
Proprietary Name: Digoxin
Non Proprietary Name: Digoxin
Active Ingredient(s): 250    ug/1 & nbsp;   Digoxin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Digoxin

Product NDC: 63629-3870
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077002
Marketing Category: ANDA
Start Marketing Date: 20071030

Package Information of Digoxin

Package NDC: 63629-3870-4
Package Description: 100 TABLET in 1 BOTTLE (63629-3870-4)

NDC Information of Digoxin

NDC Code 63629-3870-4
Proprietary Name Digoxin
Package Description 100 TABLET in 1 BOTTLE (63629-3870-4)
Product NDC 63629-3870
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071030
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name DIGOXIN
Strength Number 250
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of Digoxin


General Information