{
  "schema_version": "0.1.0",
  "id": "fda-drug-shortage:quinapril-hydrochloride-tablet",
  "slug": "quinapril-hydrochloride-tablet",
  "title": "FDA shortage status: Quinapril Hydrochloride Tablet",
  "ingredient": "Quinapril Hydrochloride Tablet",
  "status": "current",
  "source_statuses": [
    "Current",
    "To Be Discontinued"
  ],
  "brand_names": [
    "QUINAPRIL"
  ],
  "therapeutic_categories": [
    "Cardiovascular"
  ],
  "dosage_forms": [
    "Tablet"
  ],
  "routes": [
    "ORAL"
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      "product_ndc": "65862-617",
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      "manufacturer_name": "Aurobindo Pharma Limited",
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      ],
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      "initial_posting_date": "01/19/2023",
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    },
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      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "65862-620-90",
      "product_ndc": "65862-617",
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      "manufacturer_name": "Aurobindo Pharma Limited",
      "presentation": "Quinapril Hydrochloride, Tablet, 40 mg (NDC 65862-620-90)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/02/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "65862-617-90",
      "product_ndc": "65862-617",
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      "manufacturer_name": "Aurobindo Pharma Limited",
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      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/02/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "62135-485-90",
      "product_ndc": "62135-484",
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      "manufacturer_name": "Chartwell RX, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 10 mg (NDC 62135-485-90)",
      "availability": "Available",
      "dosage_form": "Tablet",
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        "ORAL"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "62135-486-90",
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      "manufacturer_name": "Chartwell RX, LLC",
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      "availability": "Available",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "62135-487-90",
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      "manufacturer_name": "Chartwell RX, LLC",
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      "update_date": "08/04/2026",
      "initial_posting_date": "01/19/2023",
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    {
      "package_ndc": "62135-484-60",
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      "manufacturer_name": "Chartwell RX, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 5 mg (NDC 62135-484-60)",
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      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "68180-557-09",
      "product_ndc": "68180-554",
      "company_name": "Lupin Pharmaceuticals, Inc.",
      "manufacturer_name": "Lupin Pharmaceuticals, Inc.",
      "presentation": "Quinapril Hydrochloride, Tablet, 10 mg (NDC 68180-557-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "08/18/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "68180-558-09",
      "product_ndc": "68180-554",
      "company_name": "Lupin Pharmaceuticals, Inc.",
      "manufacturer_name": "Lupin Pharmaceuticals, Inc.",
      "presentation": "Quinapril Hydrochloride, Tablet, 20 mg (NDC 68180-558-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "08/18/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "68180-554-09",
      "product_ndc": "68180-554",
      "company_name": "Lupin Pharmaceuticals, Inc.",
      "manufacturer_name": "Lupin Pharmaceuticals, Inc.",
      "presentation": "Quinapril Hydrochloride, Tablet, 40 mg (NDC 68180-554-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "08/18/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "68180-556-09",
      "product_ndc": null,
      "company_name": "Lupin Pharmaceuticals, Inc.",
      "manufacturer_name": null,
      "presentation": "Quinapril Hydrochloride, Tablet, 5 mg (NDC 68180-556-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "08/18/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0530-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 10 mg (NDC 0071-0530-23)",
      "availability": null,
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "10/01/2025",
      "initial_posting_date": "10/01/2025",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0530-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 10 mg (NDC 0071-0530-23)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "08/07/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0532-23",
      "product_ndc": null,
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      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 20 mg (NDC 0071-0532-23)",
      "availability": null,
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "10/01/2025",
      "initial_posting_date": "10/01/2025",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0532-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 20 mg (NDC 0071-0532-23)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "08/07/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0535-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 40 mg (NDC 0071-0535-23)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "08/07/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0535-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 40 mg (NDC 0071-0535-23)",
      "availability": null,
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "10/01/2025",
      "initial_posting_date": "10/01/2025",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0527-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 5 mg (NDC 0071-0527-23)",
      "availability": null,
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "10/01/2025",
      "initial_posting_date": "10/01/2025",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0071-0527-23",
      "product_ndc": null,
      "company_name": "Pfizer Inc.",
      "manufacturer_name": null,
      "presentation": "Accupril, Tablet, 5 mg (NDC 0071-0527-23)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [],
      "update_date": "08/07/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "43547-411-09",
      "product_ndc": "43547-410",
      "company_name": "Solco Healthcare US, LLC",
      "manufacturer_name": "Solco Healthcare US, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 10 mg (NDC 43547-411-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/29/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "43547-412-09",
      "product_ndc": "43547-410",
      "company_name": "Solco Healthcare US, LLC",
      "manufacturer_name": "Solco Healthcare US, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 20 mg (NDC 43547-412-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/29/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "43547-413-09",
      "product_ndc": "43547-410",
      "company_name": "Solco Healthcare US, LLC",
      "manufacturer_name": "Solco Healthcare US, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 40 mg (NDC 43547-413-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/29/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "43547-410-09",
      "product_ndc": "43547-410",
      "company_name": "Solco Healthcare US, LLC",
      "manufacturer_name": "Solco Healthcare US, LLC",
      "presentation": "Quinapril Hydrochloride, Tablet, 5 mg (NDC 43547-410-09)",
      "availability": "Unavailable",
      "dosage_form": "Tablet",
      "routes": [
        "ORAL"
      ],
      "update_date": "06/29/2026",
      "initial_posting_date": "01/19/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    }
  ],
  "availability_counts": {
    "Available": 4,
    "Unavailable": 16
  },
  "initial_posting_date": "01/19/2023",
  "latest_source_update": "10/01/2025",
  "source_updated_at": "2026-08-22",
  "official_url": "https://api.fda.gov/drug/shortages.json",
  "source_name": "U.S. Food and Drug Administration openFDA Drug Shortages",
  "source_license_url": "https://open.fda.gov/license/",
  "retrieved_at": "2026-08-22T15:54:11+00:00",
  "unknowns": {
    "local_availability": "Unknown. FDA status is nationwide and is not local inventory.",
    "clinical_alternatives": "Not provided. CiteFacts does not publish treatment or substitution advice.",
    "resolution_date": "Unknown unless an FDA source row provides an update date."
  },
  "derivations": {
    "status": "current when a grouped FDA row has Current; otherwise it preserves the available FDA Resolved, Discontinuation, or not-current state.",
    "ingredient_page": "Grouped by FDA generic_name, falling back to openFDA.generic_name.",
    "availability_counts": "Count of non-empty FDA package availability values; it is not a claim about local supply."
  }
}
