{
  "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": "2026-10-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "discontinued_date": "07/23/2026",
      "update_type": "New",
      "initial_posting_date": "07/23/2026",
      "package_ndc": "0574-7224-06",
      "generic_name": "Hydromorphone Hydrochloride Suppository",
      "contact_info": "(800) 775-2054",
      "related_info": "Discontinuation of the manufacture of the drug",
      "openfda": {
        "brand_name": [
          "HYDROMORPHONE HYDROCHLORIDE"
        ],
        "generic_name": [
          "HYDROMORPHONE HYDROCHLORIDE"
        ],
        "manufacturer_name": [
          "Padagis US LLC"
        ],
        "product_ndc": [
          "0574-7224"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "RECTAL"
        ],
        "substance_name": [
          "HYDROMORPHONE HYDROCHLORIDE"
        ],
        "rxcui": [
          "897749"
        ],
        "spl_id": [
          "8c369b50-cf2a-4e30-a31c-ccf5f49ab920"
        ],
        "spl_set_id": [
          "1bfbba46-1979-4797-a29e-d67718131686"
        ],
        "package_ndc": [
          "0574-7224-06"
        ],
        "unii": [
          "L960UP2KRW"
        ]
      },
      "update_date": "07/23/2026",
      "therapeutic_category": [
        "Analgesia/Addiction"
      ],
      "dosage_form": "Suppository",
      "presentation": "Hydromorphone Hydrochloride, Suppository, 3 mg (NDC 0574-7224-06)",
      "company_name": "Padagis US LLC",
      "status": "To Be Discontinued"
    }
  ]
}