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Enoxaparin sodium
Enoxaparin sodium - 0955-1016-01 - (enoxaparin sodium)
Drug Information of Enoxaparin sodium
| Product NDC: | 0955-1016 |
| Proprietary Name: | Enoxaparin sodium |
| Non Proprietary Name: | enoxaparin sodium |
| Active Ingredient(s): | 300 mg/3mL & nbsp; enoxaparin sodium |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Enoxaparin sodium
| Product NDC: | 0955-1016 |
| Labeler Name: | Winthrop U.S. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020164 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20111003 |
Package Information of Enoxaparin sodium
| Package NDC: | 0955-1016-01 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01) > 3 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Enoxaparin sodium
| NDC Code | 0955-1016-01 |
| Proprietary Name | Enoxaparin sodium |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01) > 3 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0955-1016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | enoxaparin sodium |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20111003 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Winthrop U.S. |
| Substance Name | ENOXAPARIN SODIUM |
| Strength Number | 300 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes | Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |
