{
  "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": "Newtown",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "ANDA078962"
        ],
        "brand_name": [
          "BETAXOLOL HYDROCHLORIDE"
        ],
        "generic_name": [
          "BETAXOLOL HYDROCHLORIDE"
        ],
        "manufacturer_name": [
          "KVK-TECH, INC."
        ],
        "product_ndc": [
          "10702-013",
          "10702-014"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "BETAXOLOL HYDROCHLORIDE"
        ],
        "rxcui": [
          "1297753",
          "1297757"
        ],
        "spl_id": [
          "1757ca78-c783-c977-e063-6294a90a7862"
        ],
        "spl_set_id": [
          "f3b50bbb-df03-4ed7-9d8d-180edc2abd54"
        ],
        "package_ndc": [
          "10702-013-01",
          "10702-014-01"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "6X97D2XT0O"
        ]
      },
      "product_type": "Drugs",
      "event_id": "93101",
      "recalling_firm": "KVK-Tech, Inc.",
      "address_1": "110 Terry Dr",
      "address_2": "N/A",
      "postal_code": "18940-3427",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA and PR",
      "recall_number": "D-0049-2024",
      "product_description": "Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC# 10702-013-01.",
      "product_quantity": "1488 bottles",
      "reason_for_recall": "Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.",
      "recall_initiation_date": "20230920",
      "center_classification_date": "20231018",
      "termination_date": "20250729",
      "report_date": "20231025",
      "code_info": "Lot # 17853A, Exp. 06/30/2027"
    }
  ]
}