Product NDC: | 55154-5620 |
Proprietary Name: | Jantoven |
Non Proprietary Name: | Warfarin Sodium |
Active Ingredient(s): | 5 mg/1 & nbsp; Warfarin Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-5620 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040416 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100223 |
Package NDC: | 55154-5620-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-5620-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-5620-0 |
Proprietary Name | Jantoven |
Package Description | 10 BLISTER PACK in 1 BAG (55154-5620-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-5620 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Warfarin Sodium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100223 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | WARFARIN SODIUM |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA] |