{
  "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": {
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  "results": [
    {
      "discontinued_date": "09/18/2025",
      "update_type": "New",
      "initial_posting_date": "09/18/2025",
      "package_ndc": "0832-6006-11",
      "generic_name": "Fluphenazine Hydrochloride Tablet",
      "contact_info": "763-315-2000",
      "related_info": "Discontinuation of the manufacture of the drug.",
      "openfda": {
        "application_number": [
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        "brand_name": [
          "FLUPHENAZINE HYDROCHLORIDE"
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        "generic_name": [
          "FLUPHENAZINE HYDROCHLORIDE"
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        "manufacturer_name": [
          "Upsher-Smith Laboratories,LLC"
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          "0832-6004",
          "0832-6003",
          "0832-6005"
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        "product_type": [
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        ],
        "route": [
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        "substance_name": [
          "FLUPHENAZINE HYDROCHLORIDE"
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        "rxcui": [
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          "860918",
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          "0832-6005-11",
          "0832-6006-11"
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        "unii": [
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      "update_date": "09/18/2025",
      "therapeutic_category": [
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        "Psychiatry"
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      "dosage_form": "Tablet",
      "presentation": "Fluphenazine Hydrochloride, Tablet, 10 mg (NDC 0832-6006-11)",
      "company_name": "Upsher-Smith Laboratories, LLC",
      "status": "To Be Discontinued"
    }
  ]
}