LANOXIN - 55154-0702-0 - (digoxin)

Alphabetical Index


Drug Information of LANOXIN

Product NDC: 55154-0702
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: 55154-0702
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020405
Marketing Category: NDA
Start Marketing Date: 19970930

Package Information of LANOXIN

Package NDC: 55154-0702-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0702-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of LANOXIN

NDC Code 55154-0702-0
Proprietary Name LANOXIN
Package Description 10 BLISTER PACK in 1 BAG (55154-0702-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0702
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970930
Marketing Category Name NDA
Labeler Name Cardinal Health
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