{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "update_type": "Reverified",
      "initial_posting_date": "12/30/2020",
      "package_ndc": "63323-494-05",
      "generic_name": "Valproate Sodium Injection",
      "contact_info": "888-386-1300",
      "availability": "Available",
      "related_info": "Checkwholesalers for inventory",
      "openfda": {
        "application_number": [
          "ANDA076539"
        ],
        "brand_name": [
          "VALPROATE SODIUM"
        ],
        "generic_name": [
          "VALPROATE SODIUM"
        ],
        "manufacturer_name": [
          "Fresenius Kabi USA, LLC"
        ],
        "product_ndc": [
          "63323-494"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "VALPROATE SODIUM"
        ],
        "rxcui": [
          "1099648"
        ],
        "spl_id": [
          "f09a2148-edd9-4918-8359-7554ed263d3a",
          "fff889dc-6006-43c2-be57-01b2a5724b26"
        ],
        "spl_set_id": [
          "3dfb6da1-f66a-4618-9f74-d2d6c16c0b58",
          "c572ece7-03d3-4c2a-aeb5-61f2023b28ea"
        ],
        "package_ndc": [
          "63323-494-41",
          "63323-494-16",
          "63323-494-01",
          "63323-494-05"
        ],
        "unii": [
          "5VOM6GYJ0D"
        ]
      },
      "update_date": "08/25/2026",
      "therapeutic_category": [
        "Neurology"
      ],
      "dosage_form": "Injection",
      "presentation": "Valproate Sodium, Injection, 100 mg/1 mL (NDC 63323-494-05)",
      "company_name": "Fresenius Kabi USA, LLC",
      "status": "Current"
    }
  ]
}