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ARIXTRA
ARIXTRA - 54868-5501-0 - (fondaparinux sodium)
Drug Information of ARIXTRA
| Product NDC: | 54868-5501 |
| Proprietary Name: | ARIXTRA |
| Non Proprietary Name: | fondaparinux sodium |
| Active Ingredient(s): | 7.5 mg/.6mL & nbsp; fondaparinux sodium |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARIXTRA
| Product NDC: | 54868-5501 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021345 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041117 |
Package Information of ARIXTRA
| Package NDC: | 54868-5501-0 |
| Package Description: | 10 SYRINGE in 1 CARTON (54868-5501-0) > .6 mL in 1 SYRINGE |
NDC Information of ARIXTRA
| NDC Code | 54868-5501-0 |
| Proprietary Name | ARIXTRA |
| Package Description | 10 SYRINGE in 1 CARTON (54868-5501-0) > .6 mL in 1 SYRINGE |
| Product NDC | 54868-5501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fondaparinux sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20041117 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FONDAPARINUX SODIUM |
| Strength Number | 7.5 |
| Strength Unit | mg/.6mL |
| Pharmaceutical Classes | Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA] |
