| NDC Code | 51662-1578-1 |
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| Package Description | 250 mL in 1 BAG (51662-1578-1) |
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| Product NDC | 51662-1578 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Heparin Sodium In Sodium Chloride |
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| Non-Proprietary Name | Heparin Sodium In Sodium Chloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210715 |
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| Marketing Category Name | NDA |
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| Application Number | NDA017029 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | HEPARIN SODIUM |
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| Strength | 10000 |
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| Strength Unit | [USP'U]/100mL |
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| Pharmacy Classes | Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC] |
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