{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Seymour",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA203899"
        ],
        "brand_name": [
          "NIACIN"
        ],
        "generic_name": [
          "NIACIN"
        ],
        "manufacturer_name": [
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        ],
        "product_ndc": [
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          "62175-322"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
          "NIACIN"
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        "rxcui": [
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          "1098141"
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          "62175-320-43",
          "62175-322-46",
          "62175-322-43"
        ],
        "is_original_packager": [
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        ],
        "upc": [
          "0362175320469"
        ],
        "nui": [
          "N0000175594",
          "M0014839"
        ],
        "pharm_class_epc": [
          "Nicotinic Acid [EPC]"
        ],
        "pharm_class_cs": [
          "Nicotinic Acids [CS]"
        ],
        "unii": [
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        ]
      },
      "product_type": "Drugs",
      "event_id": "97778",
      "recalling_firm": "Lannett Company Inc.",
      "address_1": "1101 C Ave W",
      "address_2": "",
      "postal_code": "47274-3342",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0096-2026",
      "product_description": "Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136.  NDC:  62175-322-46",
      "product_quantity": "46,848 90-count bottles",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20251010",
      "center_classification_date": "20251022",
      "report_date": "20251029",
      "code_info": "Lot, expiry: 21264027A, Exp 10/30/2025; 22266446A, Exp 12/31/2025; 22266901A, Exp 02/28/2026; 22267553A, 22267554A,  Exp 03/31/2026; 22267555A, Exp 02/28/2026; 22267992A, Exp 04/30/2026; 22267993A, 22267994A, Exp 05/31/2026",
      "more_code_info": ""
    }
  ]
}