{
  "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": "2026-10-22",
    "results": {
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  "results": [
    {
      "discontinued_date": "01/27/2026",
      "update_type": "New",
      "initial_posting_date": "01/27/2026",
      "package_ndc": "63323-970-02",
      "generic_name": "Benztropine Mesylate Injection",
      "contact_info": "888-386-1300",
      "related_info": "Discontinuation of the manufacture of the drug",
      "openfda": {
        "application_number": [
          "ANDA090233"
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        "brand_name": [
          "BENZTROPINE MESYLATE"
        ],
        "generic_name": [
          "BENZTROPINE MESYLATE"
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        "manufacturer_name": [
          "Fresenius Kabi USA, LLC"
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        "product_ndc": [
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        "product_type": [
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        "route": [
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          "INTRAVENOUS"
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        "substance_name": [
          "BENZTROPINE MESYLATE"
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      "update_date": "01/27/2026",
      "therapeutic_category": [
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      "dosage_form": "Injection",
      "presentation": "Benztropine Mesylate, Injection, 1 mg/1 mL (NDC 63323-970-02)",
      "company_name": "Fresenius Kabi USA, LLC",
      "status": "To Be Discontinued"
    }
  ]
}