| NDC Code | 0517-2096-25 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2096-25) > 20 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 0517-2096 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Acetate |
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| Non-Proprietary Name | Sodium Acetate |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19900930 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | American Regent, Inc. |
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| Substance Name | SODIUM ACETATE ANHYDROUS |
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| Strength | 164 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
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