| NDC Code | 0264-7652-00 |
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| Package Description | 12 CONTAINER in 1 CASE (0264-7652-00) / 1000 mL in 1 CONTAINER |
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| Product NDC | 0264-7652 |
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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, Sodium Chloride, And Potassium Chloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19880217 |
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| Marketing Category Name | NDA |
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| Application Number | NDA019630 |
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| Manufacturer | B. Braun Medical Inc. |
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| Substance Name | DEXTROSE, UNSPECIFIED FORM; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
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| Strength | 5; .15; .9 |
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| Strength Unit | g/100mL; g/100mL; g/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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