{
  "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": "2026-09-25",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "57237-106",
      "generic_name": "Divalproex Sodium",
      "labeler_name": "Rising Pharma Holdings, Inc.",
      "brand_name": "Divalproex Sodium",
      "active_ingredients": [
        {
          "name": "DIVALPROEX SODIUM",
          "strength": "125 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "57237-106-01",
          "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-01)",
          "marketing_start_date": "20141024",
          "sample": false
        },
        {
          "package_ndc": "57237-106-05",
          "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)",
          "marketing_start_date": "20141024",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Rising Pharma Holdings, Inc."
        ],
        "rxcui": [
          "1099625",
          "1099678",
          "1099870"
        ],
        "spl_set_id": [
          "6316061c-9758-4f38-9cb2-7ca833dd20bf"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "644VL95AO6"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, DELAYED RELEASE",
      "spl_id": "3664094d-b13a-4476-842b-3c56298a92fd",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20141024",
      "product_id": "57237-106_3664094d-b13a-4476-842b-3c56298a92fd",
      "application_number": "ANDA090554",
      "brand_name_base": "Divalproex Sodium",
      "pharm_class": [
        "Anti-epileptic Agent [EPC]",
        "Decreased Central Nervous System Disorganized Electrical Activity [PE]",
        "Mood Stabilizer [EPC]"
      ]
    }
  ]
}