{
  "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": "2026-09-29",
    "results": {
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  "results": [
    {
      "product_ndc": "63304-987",
      "generic_name": "Potassium Chloride",
      "labeler_name": "Sun Pharmaceutical Industries, Inc.",
      "brand_name": "Potassium Chloride",
      "active_ingredients": [
        {
          "name": "POTASSIUM CHLORIDE",
          "strength": "20 meq/1"
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          "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-987-01)",
          "marketing_start_date": "20231114",
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        },
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          "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-987-05)",
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          "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-987-10)",
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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        ],
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        "spl_set_id": [
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      "product_id": "63304-987_0a1f3d5d-13ce-97b3-e063-6394a90aa250",
      "application_number": "ANDA076368",
      "brand_name_base": "Potassium Chloride",
      "pharm_class": [
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        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Osmotic Activity [MoA]",
        "Osmotic Laxative [EPC]",
        "Potassium Compounds [CS]",
        "Potassium Salt [EPC]"
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}