Product NDC: | 55154-9359 |
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) |
Product NDC: | 55154-9359 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017029 |
Marketing Category: | NDA |
Start Marketing Date: | 20100618 |
Package NDC: | 55154-9359-5 |
Package Description: | 5 VIAL in 1 BAG (55154-9359-5) > 1 mL in 1 VIAL |
NDC Code | 55154-9359-5 |
Proprietary Name | Heparin Sodium |
Package Description | 5 VIAL in 1 BAG (55154-9359-5) > 1 mL in 1 VIAL |
Product NDC | 55154-9359 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HEPARIN SODIUM |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20100618 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | HEPARIN SODIUM |
Strength Number | 10000 |
Strength Unit | [USP'U]/mL |
Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |