DIGOX - 0527-1325-01 - (Digoxin)

Alphabetical Index


Drug Information of DIGOX

Product NDC: 0527-1325
Proprietary Name: DIGOX
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 DIGOX

Product NDC: 0527-1325
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076268
Marketing Category: ANDA
Start Marketing Date: 20020726

Package Information of DIGOX

Package NDC: 0527-1325-01
Package Description: 100 TABLET in 1 BOTTLE (0527-1325-01)

NDC Information of DIGOX

NDC Code 0527-1325-01
Proprietary Name DIGOX
Package Description 100 TABLET in 1 BOTTLE (0527-1325-01)
Product NDC 0527-1325
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020726
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name DIGOXIN
Strength Number 250
Strength Unit ug/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of DIGOX


General Information