Product NDC: | 0338-0552 |
Proprietary Name: | Heparin Sodium in Dextrose |
Non Proprietary Name: | HEPARIN SODIUM |
Active Ingredient(s): | 10000 [USP'U]/100mL & nbsp; HEPARIN SODIUM |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-0552 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018814 |
Marketing Category: | NDA |
Start Marketing Date: | 20101231 |
Package NDC: | 0338-0552-02 |
Package Description: | 250 mL in 1 BAG (0338-0552-02) |
NDC Code | 0338-0552-02 |
Proprietary Name | Heparin Sodium in Dextrose |
Package Description | 250 mL in 1 BAG (0338-0552-02) |
Product NDC | 0338-0552 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HEPARIN SODIUM |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20101231 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | HEPARIN SODIUM |
Strength Number | 10000 |
Strength Unit | [USP'U]/100mL |
Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |