| NDC Code | 63323-869-10 |
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| Package Description | 10 BAG in 1 CASE (63323-869-10) / 1000 mL in 1 BAG (63323-869-01) |
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| Product NDC | 63323-869 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dextrose And Sodium Chloride |
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| Non-Proprietary Name | Dextrose Monohydrate And Sodium Chloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20201026 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211276 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE |
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| Strength | 5; .45 |
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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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