{
  "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": "2026-09-25",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "product_ndc": "0990-7904",
      "generic_name": "DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE",
      "labeler_name": "ICU Medical Inc.",
      "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride",
      "active_ingredients": [
        {
          "name": "DEXTROSE MONOHYDRATE",
          "strength": "50 g/1000mL"
        },
        {
          "name": "SODIUM CHLORIDE",
          "strength": "4.5 g/1000mL"
        },
        {
          "name": "POTASSIUM CHLORIDE",
          "strength": "2.98 g/1000mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "0990-7904-09",
          "description": "12 POUCH in 1 CASE (0990-7904-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG",
          "marketing_start_date": "20200201",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "ICU Medical Inc."
        ],
        "rxcui": [
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          "615100",
          "615107",
          "615111",
          "630796",
          "1863605",
          "1863607",
          "1863973"
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        "spl_set_id": [
          "d8ee14e9-6733-4813-9f21-2b043a5f7188"
        ],
        "is_original_packager": [
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        "unii": [
          "LX22YL083G",
          "660YQ98I10",
          "451W47IQ8X"
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      },
      "marketing_category": "NDA",
      "dosage_form": "INJECTION, SOLUTION",
      "spl_id": "11a3a5e5-57e6-49b9-bed9-c4db277a38be",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
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      "marketing_start_date": "20200201",
      "product_id": "0990-7904_11a3a5e5-57e6-49b9-bed9-c4db277a38be",
      "application_number": "NDA018362",
      "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride",
      "pharm_class": [
        "Increased Large Intestinal Motility [PE]",
        "Increased Large Intestinal Motility [PE]",
        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Osmotic Activity [MoA]",
        "Osmotic Activity [MoA]",
        "Osmotic Laxative [EPC]",
        "Osmotic Laxative [EPC]",
        "Potassium Compounds [CS]",
        "Potassium Salt [EPC]"
      ]
    }
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}