| NDC Code | 0338-9799-12 |
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| Package Description | 12 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01) |
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| Product NDC | 0338-9799 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Glucose And Sodium Chloride |
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| Non-Proprietary Name | Dextrose Anhydrous And Sodium Chloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20241011 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | Baxter Healthcare Corporation |
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| Substance Name | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE |
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| Strength | 5.5; .9 |
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| Strength Unit | g/100mL; g/100mL |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
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