{
  "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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    {
      "status": "Terminated",
      "city": "Brookhaven",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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          "65162-757-50"
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        "is_original_packager": [
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      },
      "product_type": "Drugs",
      "event_id": "90680",
      "recalling_firm": "Amneal Pharmaceuticals of New York, LLC",
      "address_1": "50 Horseblock Rd",
      "address_2": "",
      "postal_code": "11719-9509",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "USA nationwide",
      "recall_number": "D-1362-2022",
      "product_description": "Divalproex Sodium Extended Release Tablets, USP, 250 mg, packaged in 100-count bottle, Rx only, Manufactured by: Amneal Pharmaceuticals, India, Distributed by: Amneal Pharmaceuticals, Bridgewater, NJ, NDC 65162-755-10",
      "product_quantity": "4,309 bottles",
      "reason_for_recall": "Failed dissolution specifications.",
      "recall_initiation_date": "20220727",
      "center_classification_date": "20220819",
      "termination_date": "20230817",
      "report_date": "20220831",
      "code_info": "Lot #: AR210705, Exp 04/2024",
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}