{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Central Islip",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA207418"
        ],
        "brand_name": [
          "OXYCODONE HYDROCHLORIDE"
        ],
        "generic_name": [
          "OXYCODONE HYDROCHLORIDE"
        ],
        "manufacturer_name": [
          "Camber Pharmaceuticals Inc"
        ],
        "product_ndc": [
          "31722-484",
          "31722-485",
          "31722-917",
          "31722-486",
          "31722-918"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "OXYCODONE HYDROCHLORIDE"
        ],
        "rxcui": [
          "1049611",
          "1049618",
          "1049621",
          "1049683",
          "1049686"
        ],
        "spl_id": [
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        "spl_set_id": [
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        ],
        "package_ndc": [
          "31722-484-01",
          "31722-484-05",
          "31722-485-01",
          "31722-485-05",
          "31722-917-01",
          "31722-917-05",
          "31722-486-01",
          "31722-486-05",
          "31722-918-01",
          "31722-918-05"
        ],
        "is_original_packager": [
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        "upc": [
          "0331722917018",
          "0331722485050",
          "0331722486019",
          "0331722918053",
          "0331722484053",
          "0331722486057",
          "0331722485012",
          "0331722917056",
          "0331722484015",
          "0331722918015"
        ],
        "unii": [
          "C1ENJ2TE6C"
        ]
      },
      "product_type": "Drugs",
      "event_id": "78990",
      "recalling_firm": "Ascent Pharmaceuticals, Inc.",
      "address_1": "550 S Research Pl",
      "address_2": "",
      "postal_code": "11722-4415",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0248-2018",
      "product_description": "Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY --- NDC 31722-917-01",
      "product_quantity": "45,875 bottles",
      "reason_for_recall": "Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol",
      "recall_initiation_date": "20180122",
      "center_classification_date": "20180201",
      "termination_date": "20180423",
      "report_date": "20180207",
      "code_info": "Lot Numbers: 17080591 and 17080619,  exp 07/19; 17110907 and 17110908, exp 10/19; and 17120986, exp 11/19",
      "more_code_info": ""
    }
  ]
}