{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Baltimore",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA212933"
        ],
        "brand_name": [
          "PENICILLAMINE"
        ],
        "generic_name": [
          "PENICILLAMINE"
        ],
        "manufacturer_name": [
          "Lupin Pharmaceuticals, Inc."
        ],
        "product_ndc": [
          "70748-153"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "PENICILLAMINE"
        ],
        "rxcui": [
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        "spl_id": [
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        "package_ndc": [
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        ],
        "is_original_packager": [
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        ],
        "upc": [
          "0370748153017"
        ],
        "nui": [
          "N0000175713"
        ],
        "pharm_class_epc": [
          "Antirheumatic Agent [EPC]"
        ],
        "unii": [
          "GNN1DV99GX"
        ]
      },
      "product_type": "Drugs",
      "event_id": "93482",
      "recalling_firm": "Lupin Pharmaceuticals Inc.",
      "address_1": "Harborplace Tower",
      "address_2": "111 S Calvert St Fl 21st",
      "postal_code": "21202-6174",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to 3 wholesale/distributor accounts.",
      "recall_number": "D-0148-2024",
      "product_description": "Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01",
      "product_quantity": "N/A",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20231122",
      "center_classification_date": "20231213",
      "termination_date": "20240708",
      "report_date": "20231220",
      "code_info": "Lot # M200498, Exp. June 2024"
    }
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}