{
  "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": "Oklahoma City",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA203835"
        ],
        "brand_name": [
          "LOSARTAN POTASSIUM"
        ],
        "generic_name": [
          "LOSARTAN POTASSIUM"
        ],
        "manufacturer_name": [
          "PD-Rx Pharmaceuticals, Inc."
        ],
        "product_ndc": [
          "43063-854"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "LOSARTAN POTASSIUM"
        ],
        "rxcui": [
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        ],
        "spl_id": [
          "302a7ff6-a449-db29-e063-6294a90a87b6"
        ],
        "spl_set_id": [
          "abb56236-f2fe-45b5-93ac-35fd661f8992"
        ],
        "package_ndc": [
          "43063-854-60",
          "43063-854-90",
          "43063-0854-90"
        ],
        "original_packager_product_ndc": [
          "31722-701"
        ],
        "upc": [
          "0343063854907"
        ],
        "unii": [
          "3ST302B24A"
        ]
      },
      "product_type": "Drugs",
      "event_id": "87774",
      "recalling_firm": "PD-Rx Pharmaceuticals, Inc.",
      "address_1": "727 N Ann Arbor Ave",
      "address_2": "N/A",
      "postal_code": "73127-5822",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AK, AZ, CA, CO, FL, KY, MA, MI, MN, NC, OH, OR, WI, WY",
      "recall_number": "D-0341-2021",
      "product_description": "Losartan Potassium USP, 50 mg, RX Only,  Pkg By PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 60 Tablets NDC: 43063-854-60; b) 90 Tablets NDC: 43063-0854-90",
      "product_quantity": "576 bottles",
      "reason_for_recall": "CGMP deviation: Product found to contain trace amounts of NMBA",
      "recall_initiation_date": "20190308",
      "center_classification_date": "20210426",
      "termination_date": "20210616",
      "report_date": "20210505",
      "code_info": "Lots: A19B99 Exp. 11/30/2019; B19A26 Exp. 11/30/2019; B19A69 Exp. 11/30/2019; E18F12 Exp.: 09/30/19; F18A12 Exp.: 09/30/19; F18F06 Exp.: 09/30/19; G18B43 Exp.: 09/30/19; G18C43 Exp.: 09/30/19; G18F75 Exp.: 09/30/19; H18D55 Exp.: 09/30/19; I18A11 Exp.: 09/30/19; I18E32 Exp.: 09/30/19; J18A90 Exp.: 09/30/19; J18D50 Exp. 11/30/2019; L18D01 Exp. 11/30/2019",
      "more_code_info": ""
    }
  ]
}