| NDC Code | 51662-1317-1 |
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| Package Description | 500 mL in 1 CONTAINER (51662-1317-1) |
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| Product NDC | 51662-1317 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | 6% Hetastarch In 0.9% Sodium Chloride |
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| Non-Proprietary Name | 6% Hetastarch In 0.9% Sodium Chloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20181126 |
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| Marketing Category Name | ANDA |
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| Application Number | BA740193 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | HETASTARCH |
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| Strength | 6 |
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| Strength Unit | g/100mL |
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| Pharmacy Classes | Increased Intravascular Volume [PE], Osmotic Activity [MoA], Plasma Volume Expander [EPC], Starch [CS] |
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