{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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          "ANDA078761"
        ],
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        ],
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        ],
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          "63304-758",
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          "63304-453"
        ],
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          "63304-451-01",
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          "63304-453-05"
        ],
        "is_original_packager": [
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          "0363304758016",
          "0363304452013",
          "0363304450019",
          "0363304451016"
        ],
        "unii": [
          "X3P646A2J0"
        ]
      },
      "product_type": "Drugs",
      "event_id": "96242",
      "recalling_firm": "SUN PHARMACEUTICAL INDUSTRIES INC",
      "address_1": "2 Independence Way",
      "address_2": "",
      "postal_code": "08540-6620",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within in the USA.",
      "recall_number": "D-0249-2025",
      "product_description": "Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901.  Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512.  NDC 63304-452-01",
      "product_quantity": "9840 bottles",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20250206",
      "center_classification_date": "20250303",
      "report_date": "20250312",
      "code_info": "Lot #: AD16615, Exp. Date 07/2025",
      "more_code_info": ""
    }
  ]
}