{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Seymour",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA075410"
        ],
        "brand_name": [
          "OMEPRAZOLE"
        ],
        "generic_name": [
          "OMEPRAZOLE"
        ],
        "manufacturer_name": [
          "Lannett Company, Inc."
        ],
        "product_ndc": [
          "62175-114",
          "62175-118",
          "62175-136"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "OMEPRAZOLE"
        ],
        "rxcui": [
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          "199119",
          "200329"
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        "spl_set_id": [
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          "62175-118-49",
          "62175-118-32",
          "62175-118-46",
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          "62175-136-32",
          "62175-136-46",
          "62175-136-37",
          "62175-136-43",
          "62175-136-49"
        ],
        "is_original_packager": [
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        ],
        "upc": [
          "0362175136329",
          "0362175114327",
          "0362175118325"
        ],
        "nui": [
          "N0000175525",
          "N0000000147",
          "N0000182140"
        ],
        "pharm_class_epc": [
          "Proton Pump Inhibitor [EPC]"
        ],
        "pharm_class_moa": [
          "Proton Pump Inhibitors [MoA]",
          "Cytochrome P450 2C19 Inhibitors [MoA]"
        ],
        "unii": [
          "KG60484QX9"
        ]
      },
      "product_type": "Drugs",
      "event_id": "66218",
      "recalling_firm": "Kremers Urban Pharmaceuticals, Inc.",
      "address_1": "1101 C Ave W",
      "address_2": "",
      "postal_code": "47274-3342",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "KY & TN",
      "recall_number": "D-009-2014",
      "product_description": "Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Urban Pharmaceuticals Inc.  Princeton, NJ 08540, USA, NDC: 62175-118-43",
      "product_quantity": "3867 bottles",
      "reason_for_recall": "Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.",
      "recall_initiation_date": "20130916",
      "center_classification_date": "20131120",
      "termination_date": "20140509",
      "report_date": "20131127",
      "code_info": "Lot Number 59627; Expiration Date 02/2014",
      "more_code_info": ""
    }
  ]
}