Product NDC: | 62856-750 |
Proprietary Name: | Fragmin |
Non Proprietary Name: | dalteparin sodium |
Active Ingredient(s): | 7500 [iU]/.3mL & nbsp; dalteparin sodium |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62856-750 |
Labeler Name: | Eisai Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020287 |
Marketing Category: | NDA |
Start Marketing Date: | 19941222 |
Package NDC: | 62856-750-10 |
Package Description: | 10 SYRINGE in 1 CARTON (62856-750-10) > .3 mL in 1 SYRINGE (62856-750-01) |
NDC Code | 62856-750-10 |
Proprietary Name | Fragmin |
Package Description | 10 SYRINGE in 1 CARTON (62856-750-10) > .3 mL in 1 SYRINGE (62856-750-01) |
Product NDC | 62856-750 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | dalteparin sodium |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19941222 |
Marketing Category Name | NDA |
Labeler Name | Eisai Inc. |
Substance Name | DALTEPARIN SODIUM |
Strength Number | 7500 |
Strength Unit | [iU]/.3mL |
Pharmaceutical Classes | Anti-coagulant [EPC],Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |