Digoxin - 0409-2169-31 - (DIGOXIN)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 0409-2169
Proprietary Name: Digoxin
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 Digoxin

Product NDC: 0409-2169
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040093
Marketing Category: ANDA
Start Marketing Date: 20110331

Package Information of Digoxin

Package NDC: 0409-2169-31
Package Description: 10 CARTRIDGE in 1 CARTON (0409-2169-31) > 1 mL in 1 CARTRIDGE

NDC Information of Digoxin

NDC Code 0409-2169-31
Proprietary Name Digoxin
Package Description 10 CARTRIDGE in 1 CARTON (0409-2169-31) > 1 mL in 1 CARTRIDGE
Product NDC 0409-2169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIGOXIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110331
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DIGOXIN
Strength Number 250
Strength Unit ug/mL
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of Digoxin


General Information