Product NDC: | 52584-581 |
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) |
Product NDC: | 52584-581 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA005264 |
Marketing Category: | NDA |
Start Marketing Date: | 20100301 |
Package NDC: | 52584-581-02 |
Package Description: | 1 VIAL in 1 BAG (52584-581-02) > 5 mL in 1 VIAL |
NDC Code | 52584-581-02 |
Proprietary Name | Heparin Sodium |
Package Description | 1 VIAL in 1 BAG (52584-581-02) > 5 mL in 1 VIAL |
Product NDC | 52584-581 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Heparin Sodium |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100301 |
Marketing Category Name | NDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | HEPARIN SODIUM |
Strength Number | 10000 |
Strength Unit | [USP'U]/5mL |
Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |