{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Oklahoma City",
      "state": "OK",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA040886"
        ],
        "brand_name": [
          "PHENTERMINE HYDROCHLORIDE"
        ],
        "generic_name": [
          "PHENTERMINE HYDROCHLORIDE"
        ],
        "manufacturer_name": [
          "PD-Rx Pharmaceuticals, Inc."
        ],
        "product_ndc": [
          "55289-791"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "PHENTERMINE HYDROCHLORIDE"
        ],
        "rxcui": [
          "968766"
        ],
        "spl_id": [
          "419b6194-7ef1-acbc-e063-6394a90a2315"
        ],
        "spl_set_id": [
          "4000c00f-aa6c-4ea5-af0e-149dde3c74db"
        ],
        "package_ndc": [
          "55289-791-07",
          "55289-791-14",
          "55289-791-15",
          "55289-791-21",
          "55289-791-28",
          "55289-791-30",
          "55289-791-60"
        ],
        "original_packager_product_ndc": [
          "10702-026"
        ],
        "upc": [
          "0355289791607"
        ],
        "unii": [
          "0K2I505OTV"
        ]
      },
      "product_type": "Drugs",
      "event_id": "77915",
      "recalling_firm": "PD-Rx Pharmaceuticals, Inc.",
      "address_1": "727 N Ann Arbor Ave",
      "address_2": "",
      "postal_code": "73127-5822",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-1118-2017",
      "product_description": "Phentermine Capsules, 15 mg,  a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940",
      "product_quantity": "3440 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .",
      "recall_initiation_date": "20170811",
      "center_classification_date": "20170823",
      "termination_date": "20200129",
      "report_date": "20170830",
      "code_info": "Lots: a) H15E22, Exp. 8/31/17; J15E02, Exp. 10/31/17. b) J15A53, Exp. 10/31/17; D16C78, Exp.12/31/17; c)J15D54, Exp. 10/31/17; d)H15B60, Exp. 8/31/17; e) J15A49, Exp. 10/31/17; C16A14, Exp. 12/31/17.",
      "more_code_info": ""
    }
  ]
}