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Heparin Sodium
Heparin Sodium - 0409-2581-02 - (HEPARIN SODIUM)
Drug Information of Heparin Sodium
| Product NDC: | 0409-2581 |
| Proprietary Name: | Heparin Sodium |
| Non Proprietary Name: | HEPARIN SODIUM |
| Active Ingredient(s): | 10000 [USP'U]/5mL & nbsp; HEPARIN SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium
| Product NDC: | 0409-2581 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA005264 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101022 |
Package Information of Heparin Sodium
| Package NDC: | 0409-2581-02 |
| Package Description: | 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-2581-02) > 5 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
NDC Information of Heparin Sodium
| NDC Code | 0409-2581-02 |
| Proprietary Name | Heparin Sodium |
| Package Description | 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-2581-02) > 5 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
| Product NDC | 0409-2581 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HEPARIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101022 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 10000 |
| Strength Unit | [USP'U]/5mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
