{
  "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": "2026-10-21",
    "results": {
      "skip": 0,
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  "results": [
    {
      "discontinued_date": "07/23/2026",
      "update_type": "New",
      "initial_posting_date": "07/23/2026",
      "package_ndc": "63323-943-10",
      "generic_name": "Succinylcholine Chloride Injection",
      "contact_info": "888-386-1300",
      "related_info": "Discontinuation of the manufacture of the drug",
      "openfda": {
        "application_number": [
          "ANDA211346"
        ],
        "brand_name": [
          "SUCCINYLCHOLINE CHLORIDE"
        ],
        "generic_name": [
          "SUCCINYLCHOLINE CHLORIDE"
        ],
        "manufacturer_name": [
          "Fresenius Kabi USA, LLC"
        ],
        "product_ndc": [
          "63323-943"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
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        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "SUCCINYLCHOLINE CHLORIDE"
        ],
        "rxcui": [
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        "package_ndc": [
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        "unii": [
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      },
      "update_date": "07/23/2026",
      "therapeutic_category": [
        "Anesthesia"
      ],
      "dosage_form": "Injection",
      "presentation": "Succinylcholine Chloride, Injection, 20 mg/1 mL (NDC 63323-943-10)",
      "company_name": "Fresenius Kabi USA, LLC",
      "status": "To Be Discontinued"
    }
  ]
}