Digoxin - 53808-0354-1 - (DIGOXIN)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 53808-0354
Proprietary Name: Digoxin
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 Digoxin

Product NDC: 53808-0354
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA007628
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Digoxin

Package NDC: 53808-0354-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0354-1)

NDC Information of Digoxin

NDC Code 53808-0354-1
Proprietary Name Digoxin
Package Description 30 TABLET in 1 BLISTER PACK (53808-0354-1)
Product NDC 53808-0354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIGOXIN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name DIGOXIN
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of Digoxin


General Information