| Product NDC: | 62856-251 |
| Proprietary Name: | Fragmin |
| Non Proprietary Name: | dalteparin sodium |
| Active Ingredient(s): | 25000 [iU]/mL & nbsp; dalteparin sodium |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62856-251 |
| Labeler Name: | Eisai Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020287 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19941222 |
| Package NDC: | 62856-251-01 |
| Package Description: | 1 VIAL in 1 CARTON (62856-251-01) > 3.8 mL in 1 VIAL |
| NDC Code | 62856-251-01 |
| Proprietary Name | Fragmin |
| Package Description | 1 VIAL in 1 CARTON (62856-251-01) > 3.8 mL in 1 VIAL |
| Product NDC | 62856-251 |
| 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 | 25000 |
| Strength Unit | [iU]/mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |