| NDC Code | 72439-500-10 |
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| Package Description | 10 AMPULE in 1 CARTON (72439-500-10) > 10 mL in 1 AMPULE (72439-500-41) |
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| Product NDC | 72439-500 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Chloride |
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| Non-Proprietary Name | Potassium Chloride |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20180713 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | INDUSTRIA FARMACEUTICA GALENICA SENESE SRL |
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| Substance Name | POTASSIUM CHLORIDE |
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| Strength | 149 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
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