Digoxin - 54868-2134-3 - (Digoxin)

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Drug Information of Digoxin

Product NDC: 54868-2134
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: 54868-2134
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077002
Marketing Category: ANDA
Start Marketing Date: 19920922

Package Information of Digoxin

Package NDC: 54868-2134-3
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-2134-3)

NDC Information of Digoxin

NDC Code 54868-2134-3
Proprietary Name Digoxin
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-2134-3)
Product NDC 54868-2134
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920922
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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