Product NDC: | 54868-4402 |
Proprietary Name: | Warfarin Sodium |
Non Proprietary Name: | Warfarin Sodium |
Active Ingredient(s): | 4 mg/1 & nbsp; Warfarin Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4402 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040663 |
Marketing Category: | ANDA |
Start Marketing Date: | 20001115 |
Package NDC: | 54868-4402-2 |
Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (54868-4402-2) |
NDC Code | 54868-4402-2 |
Proprietary Name | Warfarin Sodium |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (54868-4402-2) |
Product NDC | 54868-4402 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Warfarin Sodium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20001115 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | WARFARIN SODIUM |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA] |