{
  "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": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "East Windsor",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
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          "70954-202-10",
          "70954-202-20",
          "70954-200-10"
        ],
        "is_original_packager": [
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        "upc": [
          "0370954201106",
          "0370954201205",
          "0370954202103",
          "0370954200109"
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        "nui": [
          "N0000175568",
          "M0003451"
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        "pharm_class_epc": [
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        "pharm_class_cs": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "94132",
      "recalling_firm": "Novitium Pharma LLC",
      "address_1": "70 Lake Dr",
      "address_2": "",
      "postal_code": "08520-5321",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0389-2024",
      "product_description": "Digoxin Tablets, USP 125mcg, (0.125 mg), 1000-count bottle, Rx Only, Manufactured by: Novitium Pharma LLC., 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-201-20",
      "product_quantity": "3,940 1000-count bottles",
      "reason_for_recall": "Cross Contamination with Other Products:(mycophenolate mofetil).",
      "recall_initiation_date": "20240304",
      "center_classification_date": "20240315",
      "termination_date": "20250321",
      "report_date": "20240327",
      "code_info": "Lot #: M23172A, Exp 01/31/2025",
      "more_code_info": ""
    }
  ]
}