{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "NDA021506"
        ],
        "brand_name": [
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        ],
        "generic_name": [
          "MICAFUNGIN SODIUM"
        ],
        "manufacturer_name": [
          "Astellas Pharma US, Inc."
        ],
        "product_ndc": [
          "0469-3211",
          "0469-3250"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
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        "substance_name": [
          "MICAFUNGIN SODIUM"
        ],
        "rxcui": [
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          "861381",
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        "spl_id": [
          "cf33a1ae-ae66-4e64-8a9b-42b81188b179"
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        "package_ndc": [
          "0469-3250-10",
          "0469-3211-10"
        ],
        "is_original_packager": [
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        ],
        "unii": [
          "IS1UP79R56"
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      },
      "product_type": "Drugs",
      "event_id": "78981",
      "recalling_firm": "Astellas Pharma US Inc",
      "address_1": "1 Astellas Way",
      "address_2": "N/A",
      "postal_code": "60062-6111",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-0548-2018",
      "product_description": "Mycamine (micafungin) for Injection 100 mg/vial Single-Dose Vial Rx only  Marketed by: Astellas Pharma US, Inc. Northbrook, IL 60062, NDC 0469-3211-10",
      "product_quantity": "63600 vials",
      "reason_for_recall": "Labeling: Label Error on Declared Strength",
      "recall_initiation_date": "20180122",
      "center_classification_date": "20180227",
      "termination_date": "20190501",
      "report_date": "20180214",
      "code_info": "Lots: F1700164 Exp. 02/20; A000000220 Exp. 06/20"
    }
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}