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Warfarin Sodium
Warfarin Sodium - 0555-0831-05 - (Warfarin Sodium)
Drug Information of Warfarin Sodium
| Product NDC: | 0555-0831 |
| Proprietary Name: | Warfarin Sodium |
| Non Proprietary Name: | Warfarin Sodium |
| Active Ingredient(s): | 1 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: | 0555-0831 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040145 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970725 |
Package Information of Warfarin Sodium
| Package NDC: | 0555-0831-05 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0555-0831-05) |
NDC Information of Warfarin Sodium
| NDC Code | 0555-0831-05 |
| Proprietary Name | Warfarin Sodium |
| Package Description | 1000 TABLET in 1 BOTTLE (0555-0831-05) |
| Product NDC | 0555-0831 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Warfarin Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970725 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | WARFARIN SODIUM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA] |
