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Heparin Sodium
Heparin Sodium - 0641-2450-55 - (Heparin Sodium)
Drug Information of Heparin Sodium
| Product NDC: | 0641-2450 |
| Proprietary Name: | Heparin Sodium |
| Non Proprietary Name: | Heparin Sodium |
| Active Ingredient(s): | 1000 [USP'U]/mL & nbsp; Heparin Sodium |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium
| Product NDC: | 0641-2450 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017037 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19720322 |
Package Information of Heparin Sodium
| Package NDC: | 0641-2450-55 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 PACKAGE (0641-2450-55) > 30 mL in 1 VIAL, MULTI-DOSE (0641-2450-30) |
NDC Information of Heparin Sodium
| NDC Code | 0641-2450-55 |
| Proprietary Name | Heparin Sodium |
| Package Description | 25 VIAL, MULTI-DOSE in 1 PACKAGE (0641-2450-55) > 30 mL in 1 VIAL, MULTI-DOSE (0641-2450-30) |
| Product NDC | 0641-2450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Heparin Sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19720322 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 1000 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
