Digoxin - 76237-146-30 - (Digoxin)

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Drug Information of Digoxin

Product NDC: 76237-146
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: 76237-146
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077002
Marketing Category: ANDA
Start Marketing Date: 20111011

Package Information of Digoxin

Package NDC: 76237-146-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-146-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Digoxin

NDC Code 76237-146-30
Proprietary Name Digoxin
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-146-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111011
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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