DIGOX - 55289-626-30 - (Digoxin)

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Drug Information of DIGOX

Product NDC: 55289-626
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: 55289-626
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076268
Marketing Category: ANDA
Start Marketing Date: 20020726

Package Information of DIGOX

Package NDC: 55289-626-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-626-30)

NDC Information of DIGOX

NDC Code 55289-626-30
Proprietary Name DIGOX
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-626-30)
Product NDC 55289-626
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 PD-Rx Pharmaceuticals, 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