| NDC Code | 51662-1421-1 |
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| Package Description | 20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1) |
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| Product NDC | 51662-1421 |
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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 | 20191018 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA080205 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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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 | 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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