DIGOX - 49349-797-02 - (Digoxin)

Alphabetical Index


Drug Information of DIGOX

Product NDC: 49349-797
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: 49349-797
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076268
Marketing Category: ANDA
Start Marketing Date: 20130305

Package Information of DIGOX

Package NDC: 49349-797-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-797-02)

NDC Information of DIGOX

NDC Code 49349-797-02
Proprietary Name DIGOX
Package Description 30 TABLET in 1 BLISTER PACK (49349-797-02)
Product NDC 49349-797
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130305
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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