{
  "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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  "results": [
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      "city": "East Brunswick",
      "state": "NJ",
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      "classification": "Class II",
      "openfda": {
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        ],
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          "16571-863-03",
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      "address_1": "2 Tower Center Blvd Ste 1401",
      "address_2": "",
      "postal_code": "08816-1149",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0222-2024",
      "product_description": "buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, 30-count bottles, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816 Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, INDIA, NDC 16571-862-03",
      "product_quantity": "47,976 bottles",
      "reason_for_recall": "Presence of Foreign Tablets/Capsules",
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      "center_classification_date": "20240111",
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}