LANOXIN - 0173-0242-55 - (digoxin)

Alphabetical Index


Drug Information of LANOXIN

Product NDC: 0173-0242
Proprietary Name: LANOXIN
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 LANOXIN

Product NDC: 0173-0242
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020405
Marketing Category: NDA
Start Marketing Date: 19840914

Package Information of LANOXIN

Package NDC: 0173-0242-55
Package Description: 100 TABLET in 1 BOTTLE (0173-0242-55)

NDC Information of LANOXIN

NDC Code 0173-0242-55
Proprietary Name LANOXIN
Package Description 100 TABLET in 1 BOTTLE (0173-0242-55)
Product NDC 0173-0242
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19840914
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name DIGOXIN
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of LANOXIN


General Information