{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hasbrouck Heights",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA079163"
        ],
        "brand_name": [
          "DIVALPROEX SODIUM"
        ],
        "generic_name": [
          "DIVALPROEX SODIUM"
        ],
        "manufacturer_name": [
          "Unichem Pharmaceuticals (USA), Inc."
        ],
        "product_ndc": [
          "29300-138",
          "29300-139",
          "29300-140"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "DIVALPROEX SODIUM"
        ],
        "rxcui": [
          "1099625",
          "1099678",
          "1099870"
        ],
        "spl_id": [
          "674e58bd-f580-4805-a7e2-febcaa37bca5"
        ],
        "spl_set_id": [
          "1ec1a441-218a-4c80-a0cb-69bcc327f472"
        ],
        "package_ndc": [
          "29300-138-01",
          "29300-138-05",
          "29300-138-10",
          "29300-139-01",
          "29300-139-05",
          "29300-139-10",
          "29300-140-01",
          "29300-140-05",
          "29300-140-10"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0329300140019"
        ],
        "unii": [
          "644VL95AO6"
        ]
      },
      "product_type": "Drugs",
      "event_id": "78786",
      "recalling_firm": "Unichem Pharmaceuticals Usa Inc",
      "address_1": "777 Terrace Ave",
      "address_2": "Suite 102",
      "postal_code": "07604-3102",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed nationwide in the USA.",
      "recall_number": "D-0228-2018",
      "product_description": "Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories Ltd. Ind. Area, Meerut Road, Ghaziabad-201 003, India. Marketed By: Unichem Pharmaceuticals (USA), Inc. Hasbrouck Heights, NJ 07604. NDC 29300-140-01",
      "product_quantity": "96,876 Bottles of 30\u0019s",
      "reason_for_recall": "Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.",
      "recall_initiation_date": "20171219",
      "center_classification_date": "20180117",
      "termination_date": "20180912",
      "report_date": "20180124",
      "code_info": "Lot: ZDPH17040"
    }
  ]
}