{
  "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": "2026-07-22",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Brookhaven",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
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        ],
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        ],
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          "65162-757"
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        "product_type": [
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        ],
        "route": [
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        "substance_name": [
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        "rxcui": [
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          "65162-757-10",
          "65162-757-50"
        ],
        "is_original_packager": [
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        "upc": [
          "0365162755107",
          "0365162757101"
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "93976",
      "recalling_firm": "Amneal Pharmaceuticals of New York, LLC",
      "address_1": "50 Horseblock Rd",
      "address_2": "N/A",
      "postal_code": "11719-9509",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed nationwide.",
      "recall_number": "D-0426-2024",
      "product_description": "Divalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 65162-755-10. NDC# 65162-755-10",
      "product_quantity": "21,452/100 count bottles",
      "reason_for_recall": "Failed dissolution specifications",
      "recall_initiation_date": "20231226",
      "center_classification_date": "20240327",
      "termination_date": "20240816",
      "report_date": "20240403",
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      "more_code_info": ""
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}