{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-05",
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      "generic_name": "Potassium Chloride",
      "labeler_name": "Bryant Ranch Prepack",
      "brand_name": "Potassium Chloride",
      "active_ingredients": [
        {
          "name": "POTASSIUM CHLORIDE",
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      "packaging": [
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          "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1)",
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          "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)",
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      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
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        ],
        "rxcui": [
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        "spl_set_id": [
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      "brand_name_base": "Potassium Chloride",
      "pharm_class": [
        "Increased Large Intestinal Motility [PE]",
        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Osmotic Activity [MoA]",
        "Osmotic Laxative [EPC]",
        "Potassium Compounds [CS]",
        "Potassium Salt [EPC]"
      ]
    }
  ]
}