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Heparin Sodium and Sodium Chloride
Heparin Sodium and Sodium Chloride - 0338-0431-03 - (HEPARIN SODIUM)
Drug Information of Heparin Sodium and Sodium Chloride
| Product NDC: | 0338-0431 |
| Proprietary Name: | Heparin Sodium and Sodium Chloride |
| Non Proprietary Name: | HEPARIN SODIUM |
| Active Ingredient(s): | 2 [USP'U]/mL & nbsp; HEPARIN SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium and Sodium Chloride
| Product NDC: | 0338-0431 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018609 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19820428 |
Package Information of Heparin Sodium and Sodium Chloride
| Package NDC: | 0338-0431-03 |
| Package Description: | 18 BAG in 1 CARTON (0338-0431-03) > 500 mL in 1 BAG |
NDC Information of Heparin Sodium and Sodium Chloride
| NDC Code | 0338-0431-03 |
| Proprietary Name | Heparin Sodium and Sodium Chloride |
| Package Description | 18 BAG in 1 CARTON (0338-0431-03) > 500 mL in 1 BAG |
| Product NDC | 0338-0431 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HEPARIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19820428 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 2 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
