{
  "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": "2026-04-01",
    "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": "72941",
      "recalling_firm": "PD-Rx Pharmaceuticals, Inc.",
      "address_1": "727 N Ann Arbor Ave",
      "address_2": "N/A",
      "postal_code": "73127-5822",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0574-2016",
      "product_description": "Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in  a) 7-count (NDC 55289-791-07), b) 14-count (NDC 55289-791-14), c) 28-count (NDC 55289-791-28), d) 30-count (NDC 55289-791-30), and e) 60-count (NDC 55289-791-60) bottles, Packaged by PD-RX Pharmaceuticals, INC Oklahoma City, OK 73127, MFG: KVK-TECH, INC Newtown, PA 18840.",
      "product_quantity": "1685 bottles",
      "reason_for_recall": "Failed impurities/Degradation specifications: out of specification results for individual unknown and total impurity at the 12th month room temperature stability test station",
      "recall_initiation_date": "20150721",
      "center_classification_date": "20160120",
      "termination_date": "20161223",
      "report_date": "20160127",
      "code_info": "Lot #: a) H14C80, Exp 08/16; I14G36, Exp 09/16; b) H14A86, Exp 07/16;  c) H14C83, Exp 08/16, K14A21, Exp 11/16; d) H14F25, Exp 08/16; e) L14C42, Exp 12/16.",
      "more_code_info": ""
    }
  ]
}