{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Hawthorne",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
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        ],
        "brand_name": [
          "CLOBETASOL PROPIONATE"
        ],
        "generic_name": [
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          "51672-1294",
          "51672-1259"
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        "product_type": [
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      },
      "product_type": "Drugs",
      "event_id": "79029",
      "recalling_firm": "Taro Pharmaceuticals U.S.A., Inc.",
      "address_1": "3 Skyline Dr",
      "address_2": "",
      "postal_code": "10532-2174",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0249-2018",
      "product_description": "Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only  Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761  Dist. by : Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532  UPC 351672125837  NDC 51672-1258-3",
      "product_quantity": "27,792 tubes",
      "reason_for_recall": "Failed Content Uniformity Specifications",
      "recall_initiation_date": "20171221",
      "center_classification_date": "20180201",
      "termination_date": "20200921",
      "report_date": "20180207",
      "code_info": "Lot 311235, exp Sept 2018",
      "more_code_info": ""
    }
  ]
}