| NDC Code | 0338-0603-03 |
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| Package Description | 500 mL in 1 BAG (0338-0603-03) |
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| Product NDC | 0338-0603 |
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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 | Potassium Chloride, 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 | 19820323 |
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| Marketing Category Name | NDA |
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| Application Number | NDA018629 |
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| Manufacturer | Baxter Healthcare Corporation |
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| Substance Name | DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
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| Strength | 5; 150; 330 |
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| Strength Unit | g/100mL; mg/100mL; mg/100mL |
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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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