LANOXIN - 0173-0249-75 - (digoxin)

Alphabetical Index


Drug Information of LANOXIN

Product NDC: 0173-0249
Proprietary Name: LANOXIN
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 LANOXIN

Product NDC: 0173-0249
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020405
Marketing Category: NDA
Start Marketing Date: 19840702

Package Information of LANOXIN

Package NDC: 0173-0249-75
Package Description: 1000 TABLET in 1 BOTTLE (0173-0249-75)

NDC Information of LANOXIN

NDC Code 0173-0249-75
Proprietary Name LANOXIN
Package Description 1000 TABLET in 1 BOTTLE (0173-0249-75)
Product NDC 0173-0249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19840702
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name DIGOXIN
Strength Number 250
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of LANOXIN


General Information