{
  "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": "2026-10-13",
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    {
      "product_ndc": "0990-7926",
      "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE",
      "labeler_name": "ICU Medical Inc.",
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      "active_ingredients": [
        {
          "name": "DEXTROSE MONOHYDRATE",
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          "name": "SODIUM CHLORIDE",
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          "description": "24 POUCH in 1 CASE (0990-7926-02)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG",
          "marketing_start_date": "20190901",
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          "description": "24 POUCH in 1 CASE (0990-7926-03)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG",
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          "description": "12 POUCH in 1 CASE (0990-7926-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG",
          "marketing_start_date": "20191201",
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      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "ICU Medical Inc."
        ],
        "rxcui": [
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        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
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}