{
  "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": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA091363"
        ],
        "brand_name": [
          "ZOLEDRONIC ACID"
        ],
        "generic_name": [
          "ZOLEDRONIC ACID"
        ],
        "manufacturer_name": [
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        ],
        "product_ndc": [
          "55111-688"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "ZOLEDRONIC ACID"
        ],
        "rxcui": [
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        ],
        "spl_id": [
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        ],
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        "package_ndc": [
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        ],
        "is_original_packager": [
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        ],
        "upc": [
          "0355111688525"
        ],
        "unii": [
          "6XC1PAD3KF"
        ]
      },
      "product_type": "Drugs",
      "event_id": "94686",
      "recalling_firm": "Dr. Reddy's Laboratories, Inc.",
      "address_1": "107 College Rd E",
      "address_2": "",
      "postal_code": "08540-6623",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0510-2024",
      "product_description": "Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52",
      "product_quantity": "13,880 vials",
      "reason_for_recall": "Lack of Assurance of Sterility: Leaking vials",
      "recall_initiation_date": "20240523",
      "center_classification_date": "20240528",
      "report_date": "20240605",
      "code_info": "Lot #: G3000010, Exp. Date 11/2025",
      "more_code_info": ""
    }
  ]
}