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Fondaparinux Sodium
Fondaparinux Sodium - 55111-679-10 - (Fondaparinux Sodium)
Drug Information of Fondaparinux Sodium
| Product NDC: | 55111-679 |
| Proprietary Name: | Fondaparinux Sodium |
| Non Proprietary Name: | Fondaparinux Sodium |
| Active Ingredient(s): | 5 mg/4mL & nbsp; Fondaparinux Sodium |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fondaparinux Sodium
| Product NDC: | 55111-679 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091316 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110714 |
Package Information of Fondaparinux Sodium
| Package NDC: | 55111-679-10 |
| Package Description: | 10 SYRINGE in 1 CARTON (55111-679-10) > .4 mL in 1 SYRINGE (55111-679-11) |
NDC Information of Fondaparinux Sodium
| NDC Code | 55111-679-10 |
| Proprietary Name | Fondaparinux Sodium |
| Package Description | 10 SYRINGE in 1 CARTON (55111-679-10) > .4 mL in 1 SYRINGE (55111-679-11) |
| Product NDC | 55111-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fondaparinux Sodium |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20110714 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | FONDAPARINUX SODIUM |
| Strength Number | 5 |
| Strength Unit | mg/4mL |
| Pharmaceutical Classes | Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA] |
