| NDC Code | 52125-352-02 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-352-02) |
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| Product NDC | 52125-352 |
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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 | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20121210 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA018279 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | POTASSIUM CHLORIDE |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Potassium Compounds [Chemical/Ingredient],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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