{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salisbury",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA201845"
        ],
        "brand_name": [
          "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE"
        ],
        "generic_name": [
          "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE"
        ],
        "manufacturer_name": [
          "Jubilant Cadista Pharmaceuticals Inc."
        ],
        "product_ndc": [
          "59746-337",
          "59746-338",
          "59746-339"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "HYDROCHLOROTHIAZIDE",
          "LOSARTAN POTASSIUM"
        ],
        "rxcui": [
          "979464",
          "979468",
          "979471"
        ],
        "spl_id": [
          "5357e5cd-0f2e-4296-8879-72e700f87d46"
        ],
        "spl_set_id": [
          "e0b74a86-3d36-1af0-e538-41b45b8d2cc3"
        ],
        "package_ndc": [
          "59746-337-30",
          "59746-337-90",
          "59746-337-01",
          "59746-337-10",
          "59746-338-30",
          "59746-338-90",
          "59746-338-01",
          "59746-338-10",
          "59746-339-30",
          "59746-339-90",
          "59746-339-01",
          "59746-339-10"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0359746338107",
          "0359746337100",
          "0359746339104"
        ],
        "nui": [
          "N0000175359",
          "N0000175419",
          "M0471776"
        ],
        "pharm_class_pe": [
          "Increased Diuresis [PE]"
        ],
        "pharm_class_epc": [
          "Thiazide Diuretic [EPC]"
        ],
        "pharm_class_cs": [
          "Thiazides [CS]"
        ],
        "unii": [
          "3ST302B24A",
          "0J48LPH2TH"
        ]
      },
      "product_type": "Drugs",
      "event_id": "68776",
      "recalling_firm": "Jubilant Cadista Pharmaceuticals Inc.",
      "address_1": "207 Kiley Dr",
      "address_2": "",
      "postal_code": "21801-2249",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-1500-2014",
      "product_description": "Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90",
      "product_quantity": "9,358 bottles",
      "reason_for_recall": "Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.",
      "recall_initiation_date": "20140711",
      "center_classification_date": "20140731",
      "termination_date": "20160915",
      "report_date": "20140806",
      "code_info": "Lot #14P0292, Exp 04/2016",
      "more_code_info": ""
    }
  ]
}