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Heparin Sodium
Heparin Sodium - 63323-459-09 - (HEPARIN SODIUM)
Drug Information of Heparin Sodium
| Product NDC: | 63323-459 |
| Proprietary Name: | Heparin Sodium |
| Non Proprietary Name: | HEPARIN SODIUM |
| Active Ingredient(s): | 10000 [USP'U]/mL & nbsp; HEPARIN SODIUM |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium
| Product NDC: | 63323-459 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017029 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110425 |
Package Information of Heparin Sodium
| Package NDC: | 63323-459-09 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-459-09) > 4 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Heparin Sodium
| NDC Code | 63323-459-09 |
| Proprietary Name | Heparin Sodium |
| Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-459-09) > 4 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-459 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HEPARIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20110425 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 10000 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
