{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA213725"
        ],
        "brand_name": [
          "PANTOPRAZOLE SODIUM"
        ],
        "generic_name": [
          "PANTOPRAZOLE SODIUM"
        ],
        "manufacturer_name": [
          "Sun Pharmaceutical Industries, Inc."
        ],
        "product_ndc": [
          "62756-071"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "PANTOPRAZOLE SODIUM"
        ],
        "rxcui": [
          "763306"
        ],
        "spl_id": [
          "d19d65d9-7bab-4a6f-9a79-ed3d32bd83d9"
        ],
        "spl_set_id": [
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        ],
        "package_ndc": [
          "62756-071-60",
          "62756-071-64"
        ],
        "is_original_packager": [
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        ],
        "upc": [
          "0362756071643"
        ],
        "unii": [
          "6871619Q5X"
        ]
      },
      "product_type": "Drugs",
      "event_id": "91146",
      "recalling_firm": "SUN PHARMACEUTICAL INDUSTRIES INC",
      "address_1": "2 Independence Way",
      "address_2": "N/A",
      "postal_code": "08540-6620",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0068-2023",
      "product_description": "Pantoprazole Sodium for Delayed-Release Oral Suspension*40 mg* suspension in apple juice or applesauce only Each packet contains 40 mg pantoprazole equivalent to 45.1 mg of pantoprazole sodium USP (sesquihydrate), Rx Only, distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, manufactured by: Sun Pharmaceutical Industries Limited Mohali, INDIA, NDC 62756-071-60",
      "product_quantity": "14, 064 (30 sachets in a carton)",
      "reason_for_recall": "Discoloration",
      "recall_initiation_date": "20220725",
      "center_classification_date": "20221122",
      "termination_date": "20230913",
      "report_date": "20221130",
      "code_info": "Lot #: MHC1317A, Exp 07/2023"
    }
  ]
}