{
  "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": "2026-10-02",
    "results": {
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  "results": [
    {
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      "generic_name": "dextromethorphan HBr, guaifenesin",
      "labeler_name": "Amazon.com Services LLC",
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        {
          "name": "GUAIFENESIN",
          "strength": "1200 mg/1"
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          "name": "DEXTROMETHORPHAN HYDROBROMIDE",
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      "packaging": [
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          "package_ndc": "72288-812-55",
          "description": "1 BOTTLE in 1 CARTON (72288-812-55)  / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE",
          "marketing_start_date": "20210713",
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          "description": "1 BOTTLE in 1 CARTON (72288-812-66)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE",
          "marketing_start_date": "20210709",
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      ],
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      "openfda": {
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          "N0000008867",
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        ],
        "pharm_class_epc": [
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        ],
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      "product_type": "HUMAN OTC DRUG",
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      "product_id": "72288-812_ac01ad52-483a-4cce-9279-51ceecada9b9",
      "application_number": "ANDA207602",
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      "pharm_class": [
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        "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]",
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}