{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Columbus",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA211143"
        ],
        "brand_name": [
          "METOPROLOL SUCCINATE"
        ],
        "generic_name": [
          "METOPROLOL SUCCINATE ER TABLETS"
        ],
        "manufacturer_name": [
          "BluePoint Laboratories"
        ],
        "product_ndc": [
          "68001-500",
          "68001-501",
          "68001-502",
          "68001-503"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "METOPROLOL SUCCINATE"
        ],
        "rxcui": [
          "866412",
          "866419",
          "866427",
          "866436"
        ],
        "spl_id": [
          "47e38e34-d590-f7ab-e063-6394a90aa6a3"
        ],
        "spl_set_id": [
          "6588d77c-090f-4722-9c91-437887d4624a"
        ],
        "package_ndc": [
          "68001-500-00",
          "68001-500-03",
          "68001-500-08",
          "68001-501-00",
          "68001-501-03",
          "68001-501-08",
          "68001-502-00",
          "68001-502-03",
          "68001-502-08",
          "68001-503-00"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0368001500005"
        ],
        "unii": [
          "TH25PD4CCB"
        ]
      },
      "product_type": "Drugs",
      "event_id": "91528",
      "recalling_firm": "Amerisource Health Services LLC",
      "address_1": "2550 John Glenn Ave Ste A",
      "address_2": "N/A",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide USA",
      "recall_number": "D-0269-2023",
      "product_description": "Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00; (b) 500-count bottle, NDC 68001-501-03. Manufactured by Alkem Laboratories Ltd., India. For BluePoint Laboratories",
      "product_quantity": "(a) 6670 100-count (b) 2666 500-count bottles",
      "reason_for_recall": "Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer  which included lots that were packaged for BluePoint Laboratories.",
      "recall_initiation_date": "20230111",
      "center_classification_date": "20230215",
      "termination_date": "20240512",
      "report_date": "20230222",
      "code_info": "Lots: (a) 21143211, EXP 03/31/2023; (b) 21143185, 21143193, EXP 02/28/2023"
    }
  ]
}