| NDC Code | 65219-142-10 |
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| Package Description | 10 BAG in 1 CASE (65219-142-10) / 1000 mL in 1 BAG (65219-142-02) |
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| Product NDC | 65219-142 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Chloride In Dextrose And Sodium Chloride |
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| Non-Proprietary Name | Dextrose Monohydrate, Sodium Chloride, And Potassium Chloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20220826 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213523 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
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| Strength | 50; .745; 4.5 |
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| Strength Unit | g/1000mL; g/1000mL; g/1000mL |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
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