{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Seymour",
      "state": "IN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA078503"
        ],
        "brand_name": [
          "OXYBUTYNIN CHLORIDE"
        ],
        "generic_name": [
          "OXYBUTYNIN CHLORIDE"
        ],
        "manufacturer_name": [
          "Lannett Company, Inc."
        ],
        "product_ndc": [
          "62175-270",
          "62175-271",
          "62175-272"
        ],
        "product_type": [
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        ],
        "route": [
          "ORAL"
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        "substance_name": [
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        "rxcui": [
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          "863628",
          "863636"
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        "spl_set_id": [
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        "package_ndc": [
          "62175-270-37",
          "62175-270-41",
          "62175-271-37",
          "62175-271-41",
          "62175-272-37",
          "62175-272-41"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "L9F3D9RENQ"
        ]
      },
      "product_type": "Drugs",
      "event_id": "82144",
      "recalling_firm": "Lannett Company Inc.",
      "address_1": "1101 C Ave W",
      "address_2": "N/A",
      "postal_code": "47274-3342",
      "voluntary_mandated": "N/A",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, including Puerto Rico.",
      "recall_number": "D-0996-2019",
      "product_description": "Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154  NDC: 62175-271-37",
      "product_quantity": "14,448 bottles",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20190221",
      "center_classification_date": "20190312",
      "termination_date": "20201106",
      "report_date": "20190320",
      "code_info": "Lots: 18226783A, exp 07/2021 and 18232540A, exp 08/2021"
    }
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}