Digoxin - 21695-678-30 - (Digoxin)

Alphabetical Index


Drug Information of Digoxin

Product NDC: 21695-678
Proprietary Name: Digoxin
Non Proprietary Name: Digoxin
Active Ingredient(s): .125    mg/1 & nbsp;   Digoxin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Digoxin

Product NDC: 21695-678
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20101001

Package Information of Digoxin

Package NDC: 21695-678-30
Package Description: 30 TABLET in 1 BOTTLE (21695-678-30)

NDC Information of Digoxin

NDC Code 21695-678-30
Proprietary Name Digoxin
Package Description 30 TABLET in 1 BOTTLE (21695-678-30)
Product NDC 21695-678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Digoxin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101001
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name DIGOXIN
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

Complete Information of Digoxin


General Information