{
  "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": "WILMINGTON",
      "state": "DE",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "NDA022101"
        ],
        "brand_name": [
          "NEXIUM"
        ],
        "generic_name": [
          "ESOMEPRAZOLE MAGNESIUM"
        ],
        "manufacturer_name": [
          "AstraZeneca Pharmaceuticals LP"
        ],
        "product_ndc": [
          "0186-4010",
          "0186-5020",
          "0186-4020",
          "0186-4040",
          "0186-5040",
          "0186-4025",
          "0186-4050"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "ESOMEPRAZOLE MAGNESIUM TRIHYDRATE"
        ],
        "rxcui": [
          "606726",
          "606728",
          "606730",
          "606731",
          "692576",
          "692578",
          "861568",
          "861570",
          "861576",
          "861583",
          "1297658",
          "1297660",
          "1297761",
          "1297763"
        ],
        "spl_id": [
          "d8251328-3547-4a76-8ec8-1b2338dbbedf"
        ],
        "spl_set_id": [
          "f4853677-1622-4037-688b-fdf533a11d96"
        ],
        "package_ndc": [
          "0186-5020-31",
          "0186-5020-54",
          "0186-5020-82",
          "0186-4010-01",
          "0186-4010-02",
          "0186-4020-01",
          "0186-4040-01",
          "0186-4040-02",
          "0186-5040-31",
          "0186-5040-35",
          "0186-5040-55",
          "0186-5040-85",
          "0186-5040-54",
          "0186-5040-82",
          "0186-5040-05",
          "0186-4025-01",
          "0186-4025-02",
          "0186-4050-01"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "R6DXU4WAY9"
        ],
        "upc": [
          "301865040850"
        ]
      },
      "product_type": "Drugs",
      "event_id": "62439",
      "recalling_firm": "ASTRA ZENECA Lp",
      "address_1": "1800 CONCORD PIKE",
      "address_2": "",
      "postal_code": "19803-2902",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-1410-2012",
      "product_description": "Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, Manufactured for: AstraZeneca LP, Wilmington, DE  19850; By: AstraZeneca AB, S-151 85 Sodertalje, Sweden, NDC 0186-5040-85, UPC 3 0186-5040-85 0.",
      "product_quantity": "2,556 bottles",
      "reason_for_recall": "Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a small number of Nexium 20 mg capsules intended for the Japanese market in addtion to Nexium 40 mg capsules.",
      "recall_initiation_date": "20120702",
      "center_classification_date": "20120711",
      "termination_date": "20130411",
      "report_date": "20120718",
      "code_info": "Lot #: H008328, Exp 11/14",
      "more_code_info": ""
    }
  ]
}