{
  "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": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA040796"
        ],
        "brand_name": [
          "FOLIC ACID"
        ],
        "generic_name": [
          "FOLIC ACID"
        ],
        "manufacturer_name": [
          "Leading Pharma, LLC"
        ],
        "product_ndc": [
          "69315-127"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "FOLIC ACID"
        ],
        "rxcui": [
          "310410"
        ],
        "spl_id": [
          "92322e52-3179-4738-8c8a-14fef62311d4"
        ],
        "spl_set_id": [
          "1ba8c407-9613-4319-ac40-0a429cb0f3f4"
        ],
        "package_ndc": [
          "69315-127-01",
          "69315-127-10"
        ],
        "is_original_packager": [
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        ],
        "unii": [
          "935E97BOY8"
        ]
      },
      "product_type": "Drugs",
      "event_id": "89450",
      "recalling_firm": "CARDINAL HEALTHCARE",
      "address_1": "7200 Cardinal Pl W",
      "address_2": "",
      "postal_code": "43017-1094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide USA",
      "recall_number": "D-0183-2024",
      "product_description": "FOLIC ACID TABLETS, USP, 1MG, 100 Tablets per bottle, Rx Only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004.  NDC: 69315-127-10",
      "product_quantity": "1 unit",
      "reason_for_recall": "CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.",
      "recall_initiation_date": "20220126",
      "center_classification_date": "20231226",
      "termination_date": "20240929",
      "report_date": "20240103",
      "code_info": "Batch H08221",
      "more_code_info": ""
    }
  ]
}