{
  "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": "2026-07-29",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        ],
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        "manufacturer_name": [
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        ],
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          "62756-797",
          "62756-798"
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "90495",
      "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 in the USA",
      "recall_number": "D-1291-2022",
      "product_description": "Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol- 389 350, Gujarat, India,  NDC 62756-798-88.",
      "product_quantity": "9552 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.",
      "recall_initiation_date": "20220627",
      "center_classification_date": "20220726",
      "termination_date": "20230531",
      "report_date": "20220803",
      "code_info": "Lot: HAC1312A, EXP. 05/2024",
      "more_code_info": ""
    }
  ]
}