| NDC Code | 10135-820-08 |
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| Package Description | 3 g in 1 BOTTLE (10135-820-08) |
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| Product NDC | 10135-820 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Chloride For Oral Solution |
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| Non-Proprietary Name | Potassium Chloride For Oral Solution |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20250801 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212183 |
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| Manufacturer | Marlex Pharmaceuticals Inc |
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| Substance Name | POTASSIUM CHLORIDE |
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| Strength | 3 |
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| Strength Unit | g/4.75g |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
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