{
  "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": [
    {
      "update_type": "Reverified",
      "initial_posting_date": "01/19/2023",
      "package_ndc": "65862-162-90",
      "generic_name": "Quinapril/Hydrochlorothiazide Tablet",
      "contact_info": "866-850-2876",
      "availability": "Unavailable",
      "related_info": "Discontinuation of the manufacture of the drug",
      "openfda": {
        "application_number": [
          "ANDA078450"
        ],
        "brand_name": [
          "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE"
        ],
        "generic_name": [
          "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE"
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        ],
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          "65862-162",
          "65862-161",
          "65862-163"
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        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
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        "route": [
          "ORAL"
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        "substance_name": [
          "QUINAPRIL HYDROCHLORIDE",
          "HYDROCHLOROTHIAZIDE"
        ],
        "rxcui": [
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          "310797",
          "310809"
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        "nui": [
          "N0000175359",
          "N0000175419",
          "M0471776"
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        "pharm_class_pe": [
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        ],
        "pharm_class_epc": [
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          "0J48LPH2TH"
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      },
      "update_date": "06/02/2026",
      "therapeutic_category": [
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      "dosage_form": "Tablet",
      "presentation": "Quinapril Hydrochloride And Hydrochlorothiazide, Tablet, 12.5 mg; 20 mg (NDC 65862-162-90)",
      "company_name": "Aurobindo Pharma USA",
      "shortage_reason": "Discontinuation of the manufacture of the drug",
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}