Product NDC: | 68084-508 |
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) |
Product NDC: | 68084-508 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077002 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110701 |
Package NDC: | 68084-508-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (68084-508-01) > 10 TABLET in 1 BLISTER PACK (68084-508-11) |
NDC Code | 68084-508-01 |
Proprietary Name | Digoxin |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-508-01) > 10 TABLET in 1 BLISTER PACK (68084-508-11) |
Product NDC | 68084-508 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Digoxin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110701 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | DIGOXIN |
Strength Number | 125 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |