{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Earth City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA076001"
        ],
        "brand_name": [
          "FLUOXETINE"
        ],
        "generic_name": [
          "FLUOXETINE"
        ],
        "manufacturer_name": [
          "Legacy Pharmaceutical Packaging, LLC"
        ],
        "product_ndc": [
          "68645-130",
          "68645-131"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "FLUOXETINE HYDROCHLORIDE"
        ],
        "rxcui": [
          "310384",
          "310385"
        ],
        "spl_id": [
          "4c222d2c-813c-5520-e063-6294a90affe6"
        ],
        "spl_set_id": [
          "b07f9eab-44ac-4667-bd46-52d736daa5d6"
        ],
        "package_ndc": [
          "68645-131-54",
          "68645-130-54"
        ],
        "original_packager_product_ndc": [
          "50111-647",
          "50111-648"
        ],
        "upc": [
          "0368645130545",
          "368645130545"
        ],
        "unii": [
          "I9W7N6B1KJ"
        ]
      },
      "product_type": "Drugs",
      "event_id": "67526",
      "recalling_firm": "Legacy Pharmaceutical Packaging",
      "address_1": "13333 Lakefront Dr",
      "address_2": "",
      "postal_code": "63045-1514",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1279-2014",
      "product_description": "Fluoxetine Capsules, USP, 20 mg, 30-count bottles, Rx only, Distributed by: Wal-Mart, Bentonville, AR  72716; Manufactured by: TEVA PHARMACEUTICALS USA, Sellersville, PA  18960; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO  63045, NDC 68645-130-54, UPC 3 68645 13054 5.",
      "product_quantity": "667,068 bottles",
      "reason_for_recall": "Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.",
      "recall_initiation_date": "20140214",
      "center_classification_date": "20140428",
      "termination_date": "20171127",
      "report_date": "20140507",
      "code_info": "Lot numbers: 131328, Exp 08/15; 131634, Exp 09/15; and 131833, Exp 11/15",
      "more_code_info": ""
    }
  ]
}