{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
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  "results": [
    {
      "status": "Terminated",
      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA090873"
        ],
        "brand_name": [
          "CLONIDINE TRANSDERMAL SYSTEM"
        ],
        "generic_name": [
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        ],
        "manufacturer_name": [
          "Actavis Pharma, Inc."
        ],
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          "0591-3508",
          "0591-3509",
          "0591-3510"
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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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          "998675",
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        "package_ndc": [
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          "0591-3508-04",
          "0591-3509-54",
          "0591-3509-04",
          "0591-3510-54",
          "0591-3510-04"
        ],
        "is_original_packager": [
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        ],
        "nui": [
          "N0000009918",
          "N0000175554"
        ],
        "pharm_class_moa": [
          "Adrenergic alpha2-Agonists [MoA]"
        ],
        "pharm_class_epc": [
          "Central alpha-2 Adrenergic Agonist [EPC]"
        ],
        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "88938",
      "recalling_firm": "Teva Pharmaceuticals USA",
      "address_1": "400 Interpace Pkwy",
      "address_2": "N/A",
      "postal_code": "07054-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0235-2022",
      "product_description": "Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 0591-3508-04",
      "product_quantity": "64,978 patches",
      "reason_for_recall": "Failed Impurities/Degradation Specifications",
      "recall_initiation_date": "20211028",
      "center_classification_date": "20211116",
      "termination_date": "20230227",
      "report_date": "20211124",
      "code_info": "Lot# 1369117B, exp. date 11/2021",
      "more_code_info": ""
    }
  ]
}