{
  "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": "2026-10-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "62135-667",
      "generic_name": "Quinapril and Hydrochlorothiazide",
      "labeler_name": "Chartwell RX, LLC",
      "brand_name": "Quinapril and Hydrochlorothiazide",
      "active_ingredients": [
        {
          "name": "QUINAPRIL HYDROCHLORIDE",
          "strength": "10 mg/1"
        },
        {
          "name": "HYDROCHLOROTHIAZIDE",
          "strength": "12.5 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "62135-667-90",
          "description": "90 TABLET in 1 BOTTLE (62135-667-90)",
          "marketing_start_date": "20231205",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Chartwell RX, LLC"
        ],
        "rxcui": [
          "310796",
          "310797",
          "310809"
        ],
        "spl_set_id": [
          "2eae533f-d0af-47e8-a1f2-94bc8cc89b5a"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0362135669904",
          "0362135667900",
          "0362135668907"
        ],
        "nui": [
          "N0000175359",
          "N0000175419",
          "M0471776"
        ],
        "pharm_class_pe": [
          "Increased Diuresis [PE]"
        ],
        "pharm_class_epc": [
          "Thiazide Diuretic [EPC]"
        ],
        "pharm_class_cs": [
          "Thiazides [CS]"
        ],
        "unii": [
          "0J48LPH2TH",
          "33067B3N2M"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET",
      "spl_id": "0c3f4504-d57e-aa79-e063-6294a90ad5b8",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20040331",
      "product_id": "62135-667_0c3f4504-d57e-aa79-e063-6294a90ad5b8",
      "application_number": "ANDA076374",
      "brand_name_base": "Quinapril and Hydrochlorothiazide",
      "pharm_class": [
        "Angiotensin Converting Enzyme Inhibitor [EPC]",
        "Angiotensin-converting Enzyme Inhibitors [MoA]",
        "Increased Diuresis [PE]",
        "Thiazide Diuretic [EPC]",
        "Thiazides [CS]"
      ]
    }
  ]
}