{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Baltimore",
      "state": "MD",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA090694"
        ],
        "brand_name": [
          "DULOXETINE"
        ],
        "generic_name": [
          "DULOXETINE"
        ],
        "manufacturer_name": [
          "Lupin Pharmaceuticals, Inc."
        ],
        "product_ndc": [
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          "68180-295",
          "68180-296",
          "68180-297"
        ],
        "product_type": [
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        ],
        "route": [
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        ],
        "substance_name": [
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        ],
        "rxcui": [
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          "596930",
          "596934",
          "616402"
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        "spl_id": [
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        "spl_set_id": [
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          "68180-294-03",
          "68180-294-09",
          "68180-294-06",
          "68180-295-06",
          "68180-295-09",
          "68180-295-03",
          "68180-296-03",
          "68180-296-06",
          "68180-296-09",
          "68180-297-06",
          "68180-297-09",
          "68180-297-03",
          "3681802950"
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        "is_original_packager": [
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        "unii": [
          "9044SC542W"
        ],
        "upc": [
          "368180295068"
        ]
      },
      "product_type": "Drugs",
      "event_id": "78596",
      "recalling_firm": "Lupin Pharmaceuticals Inc.",
      "address_1": "111 S Calvert St Fl 21ST",
      "address_2": "N/A",
      "postal_code": "21202-6174",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0097-2018",
      "product_description": "Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Goa 403 722 India, NDC 68180-295-06, UPC 368180295068",
      "product_quantity": "111,648 units",
      "reason_for_recall": "Failed Dissolution Specification",
      "recall_initiation_date": "20171121",
      "center_classification_date": "20171128",
      "termination_date": "20190415",
      "report_date": "20171206",
      "code_info": "Lot #: G602051, Exp. 12/2017"
    }
  ]
}