{
  "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": [
    {
      "product_ndc": "75907-431",
      "generic_name": "Acetaminophen Diphenhydramine HCL",
      "labeler_name": "Dr. Reddy's Laboratories Inc.",
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      "active_ingredients": [
        {
          "name": "ACETAMINOPHEN",
          "strength": "500 mg/1"
        },
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          "strength": "25 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "75907-431-01",
          "description": "1 BOTTLE in 1 CARTON (75907-431-01)  / 100 TABLET in 1 BOTTLE",
          "marketing_start_date": "20260925",
          "sample": false
        },
        {
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          "description": "300 TABLET in 1 BOTTLE (75907-431-30)",
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          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {},
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      "dosage_form": "TABLET",
      "spl_id": "d948fa6f-21f3-1861-6421-e5642bf8e4d3",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "75907-431_d948fa6f-21f3-1861-6421-e5642bf8e4d3",
      "application_number": "M013",
      "brand_name_base": "Acetaminophen Diphenhydramine HCL",
      "pharm_class": [
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        "Histamine-1 Receptor Antagonist [EPC]"
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}