LANOXIN - 0173-0260-10 - (digoxin)

Alphabetical Index


Drug Information of LANOXIN

Product NDC: 0173-0260
Proprietary Name: LANOXIN
Non Proprietary Name: digoxin
Active Ingredient(s): 250    ug/mL & nbsp;   digoxin
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LANOXIN

Product NDC: 0173-0260
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009330
Marketing Category: NDA
Start Marketing Date: 19851001

Package Information of LANOXIN

Package NDC: 0173-0260-10
Package Description: 10 AMPULE in 1 BOX (0173-0260-10) > 2 mL in 1 AMPULE

NDC Information of LANOXIN

NDC Code 0173-0260-10
Proprietary Name LANOXIN
Package Description 10 AMPULE in 1 BOX (0173-0260-10) > 2 mL in 1 AMPULE
Product NDC 0173-0260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name digoxin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19851001
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name DIGOXIN
Strength Number 250
Strength Unit ug/mL
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of LANOXIN


General Information