{
  "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": "2026-08-12",
    "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": [
          "ANDA078853"
        ],
        "brand_name": [
          "DIVALPROEX SODIUM"
        ],
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          "DIVALPROEX SODIUM"
        ],
        "manufacturer_name": [
          "Bionpharma Inc."
        ],
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          "69452-433",
          "69452-434",
          "69452-435"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
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        "rxcui": [
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          "1099678",
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        "spl_id": [
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        "spl_set_id": [
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        "package_ndc": [
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          "69452-433-20",
          "69452-433-30",
          "69452-434-13",
          "69452-434-20",
          "69452-434-30",
          "69452-435-13",
          "69452-435-20",
          "69452-435-30"
        ],
        "is_original_packager": [
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        "unii": [
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        ]
      },
      "product_type": "Drugs",
      "event_id": "99316",
      "recalling_firm": "Bionpharma Inc.",
      "address_1": "400 Alexander Park Ste 2-4b",
      "address_2": "N/A",
      "postal_code": "08540-6539",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide.",
      "recall_number": "D-0742-2026",
      "product_description": "Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, Made in India, NDC 69452-435-30.",
      "product_quantity": "N/A",
      "reason_for_recall": "Presence of Foreign Tablets/Capsules",
      "recall_initiation_date": "20260626",
      "center_classification_date": "20260806",
      "report_date": "20260729",
      "code_info": "Lot# 704C003, Exp. 12/31/2028"
    }
  ]
}