{
  "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": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA091220"
        ],
        "brand_name": [
          "GLIMEPIRIDE"
        ],
        "generic_name": [
          "GLIMEPIRIDE"
        ],
        "manufacturer_name": [
          "Micro Labs Limited"
        ],
        "product_ndc": [
          "42571-100",
          "42571-101",
          "42571-102",
          "42571-103",
          "42571-104",
          "42571-105"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "GLIMEPIRIDE"
        ],
        "rxcui": [
          "153842",
          "199245",
          "199246",
          "199247",
          "1361493",
          "1361495"
        ],
        "spl_id": [
          "34e9a6b6-450b-7d20-e063-6294a90ac831"
        ],
        "spl_set_id": [
          "60e9397e-83b9-489e-9683-6f87e458bbaa"
        ],
        "package_ndc": [
          "42571-100-01",
          "42571-100-05",
          "42571-101-01",
          "42571-101-05",
          "42571-102-01",
          "42571-102-05",
          "42571-103-01",
          "42571-103-05",
          "42571-104-01",
          "42571-104-05",
          "42571-105-01",
          "42571-105-05"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0342571100018",
          "0342571102012",
          "0342571101015",
          "0342571104016",
          "0342571105013",
          "0342571103019"
        ],
        "nui": [
          "N0000175608",
          "M0020795"
        ],
        "pharm_class_epc": [
          "Sulfonylurea [EPC]"
        ],
        "pharm_class_cs": [
          "Sulfonylurea Compounds [CS]"
        ],
        "unii": [
          "6KY687524K"
        ]
      },
      "product_type": "Drugs",
      "event_id": "69133",
      "recalling_firm": "Micro Labs Usa, Inc                                    S",
      "address_1": "104 Carnegie Ctr",
      "address_2": "Te 216",
      "postal_code": "08540-6232",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CT, FL, MD, MS, NY",
      "recall_number": "D-0046-2015",
      "product_description": "GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b)  500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs Limited, Goa-403 722, INDIA, Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540",
      "product_quantity": "11,328 bottles",
      "reason_for_recall": "Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.",
      "recall_initiation_date": "20141009",
      "center_classification_date": "20141027",
      "termination_date": "20151229",
      "report_date": "20141105",
      "code_info": "GLBG001 Exp.12/14, GLBG008 Exp. 06/15",
      "more_code_info": ""
    }
  ]
}