Digoxin - 51079-847-20 - (Digoxin)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 51079-847
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: 51079-847
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077002
Marketing Category: ANDA
Start Marketing Date: 20110429

Package Information of Digoxin

Package NDC: 51079-847-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-847-20) > 1 TABLET in 1 BLISTER PACK (51079-847-01)

NDC Information of Digoxin

NDC Code 51079-847-20
Proprietary Name Digoxin
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-847-20) > 1 TABLET in 1 BLISTER PACK (51079-847-01)
Product NDC 51079-847
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110429
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
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