{
  "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": "2026-07-08",
    "results": {
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  },
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    {
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      "city": "Mumbai",
      "state": "",
      "country": "India",
      "classification": "Class II",
      "openfda": {
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        "manufacturer_name": [
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          "33342-068",
          "33342-069",
          "33342-070",
          "33342-071",
          "33342-072"
        ],
        "product_type": [
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        ],
        "route": [
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        "substance_name": [
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        "rxcui": [
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        ],
        "is_original_packager": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "95838",
      "recalling_firm": "Macleods Pharmaceuticals Ltd",
      "address_1": "304 Atlanta Arcade",
      "address_2": "Church Road",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0154-2025",
      "product_description": "Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540, Manufactured for: Macleods Pharma USA Inc. Princeton, NJ,08540: Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi Himachal Pradesh, INDIA, NDC 33342-067-07.",
      "product_quantity": "15,744 30-count bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications",
      "recall_initiation_date": "20241125",
      "center_classification_date": "20241219",
      "report_date": "20241225",
      "code_info": "Lot# BOB12318A Exp 07/31/2027",
      "more_code_info": ""
    }
  ]
}