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COUMADIN
COUMADIN - 52125-080-02 - (warfarin sodium)
Drug Information of COUMADIN
| Product NDC: | 52125-080 |
| Proprietary Name: | COUMADIN |
| 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) |
Labeler Information of COUMADIN
| Product NDC: | 52125-080 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA009218 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130226 |
Package Information of COUMADIN
| Package NDC: | 52125-080-02 |
| Package Description: | 100 TABLET in 1 BLISTER PACK (52125-080-02) |
NDC Information of COUMADIN
| NDC Code | 52125-080-02 |
| Proprietary Name | COUMADIN |
| Package Description | 100 TABLET in 1 BLISTER PACK (52125-080-02) |
| Product NDC | 52125-080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | warfarin sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130226 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | WARFARIN SODIUM |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA] |
