{
  "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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    {
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      "generic_name": "Ibuprofen and Diphenhydramine Citrate",
      "labeler_name": "Kenvue Brands LLC",
      "brand_name": "Motrin PM",
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          "name": "IBUPROFEN",
          "strength": "200 mg/1"
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          "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-563-20)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC",
          "marketing_start_date": "20100111",
          "sample": false
        },
        {
          "package_ndc": "50580-563-80",
          "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-563-80)  / 80 TABLET, COATED in 1 BOTTLE, PLASTIC",
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      ],
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      "openfda": {
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      "dosage_form": "TABLET, COATED",
      "spl_id": "39a34ab2-9fae-444e-e063-6294a90a9152",
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        "Cyclooxygenase Inhibitors [MoA]",
        "Histamine H1 Receptor Antagonists [MoA]",
        "Histamine-1 Receptor Antagonist [EPC]",
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}