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Warfarin Sodium
Warfarin Sodium - 51672-4035-3 - (Warfarin Sodium)
Drug Information of Warfarin Sodium
| Product NDC: | 51672-4035 |
| Proprietary Name: | Warfarin Sodium |
| Non Proprietary Name: | Warfarin Sodium |
| Active Ingredient(s): | 10 mg/1 & nbsp; Warfarin Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Warfarin Sodium
| Product NDC: | 51672-4035 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040301 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990715 |
Package Information of Warfarin Sodium
| Package NDC: | 51672-4035-3 |
| Package Description: | 1000 TABLET in 1 BOTTLE (51672-4035-3) |
NDC Information of Warfarin Sodium
| NDC Code | 51672-4035-3 |
| Proprietary Name | Warfarin Sodium |
| Package Description | 1000 TABLET in 1 BOTTLE (51672-4035-3) |
| Product NDC | 51672-4035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Warfarin Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990715 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | WARFARIN SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA] |
