{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Glasgow",
      "state": "KY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA075022",
          "ANDA077321"
        ],
        "brand_name": [
          "BUSPIRONE HYDROCHLORIDE",
          "LISINOPRIL"
        ],
        "generic_name": [
          "BUSPIRONE HYDROCHLORIDE",
          "LISINOPRIL"
        ],
        "manufacturer_name": [
          "NCS HealthCare of KY, LLC dba Vangard Labs"
        ],
        "product_ndc": [
          "0615-7689",
          "0615-7714",
          "0615-7718",
          "0615-8252",
          "0615-8253",
          "0615-8256",
          "0615-8254",
          "0615-8255"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "BUSPIRONE HYDROCHLORIDE",
          "LISINOPRIL"
        ],
        "rxcui": [
          "866018",
          "866083",
          "866094",
          "197884",
          "311353",
          "311354",
          "314076",
          "314077"
        ],
        "spl_id": [
          "77cbe6b7-dd55-4745-a49e-1e22072beccd",
          "e5a3bed2-db01-4bc5-b231-ff76cecb7225"
        ],
        "spl_set_id": [
          "72bff09c-826e-4394-a7e7-41d56ce9605b",
          "43fa9a16-c112-419f-8d7b-177f580462f2"
        ],
        "package_ndc": [
          "0615-7714-39",
          "0615-7714-05",
          "0615-7714-30",
          "0615-7718-39",
          "0615-7718-31",
          "0615-7718-05",
          "0615-7718-28",
          "0615-7689-39",
          "0615-7689-31",
          "0615-7689-05",
          "0615-8252-39",
          "0615-8252-05",
          "0615-8253-39",
          "0615-8253-05",
          "0615-8253-30",
          "0615-8256-39",
          "0615-8256-05",
          "0615-8254-39",
          "0615-8254-05",
          "0615-8254-30",
          "0615-8255-39",
          "0615-8255-05",
          "0615-8255-30"
        ],
        "original_packager_product_ndc": [
          "0093-0053",
          "0093-0054",
          "0093-1003",
          "68180-512",
          "68180-513",
          "68180-517",
          "68180-980",
          "68180-981"
        ],
        "unii": [
          "207LT9J9OC",
          "E7199S1YWR"
        ]
      },
      "product_type": "Drugs",
      "event_id": "93336",
      "recalling_firm": "NCS Healthcare of Kentucky Inc",
      "address_1": "120 Carroll Knicely Dr",
      "address_2": "N/A",
      "postal_code": "42141-7224",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide USA",
      "recall_number": "D-0114-2024",
      "product_description": "Lisinopril Tablets USP 20 mg, packaged in a) 15-count blister card (NDC 0615-7718-05), b) 30-count blister card (NDC 0615-8255-39), Rx only, Mfd By Lupin, PKG by Vangard Glasgow, KY 42141.",
      "product_quantity": "12 cards",
      "reason_for_recall": "Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots",
      "recall_initiation_date": "20231027",
      "center_classification_date": "20231121",
      "termination_date": "20240714",
      "report_date": "20231129",
      "code_info": "Lot#: a) 8255-3012, Exp 08/31/2024; b) 8255-3012, Exp 08/31/2024",
      "more_code_info": ""
    }
  ]
}