{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "71288-035",
      "generic_name": "fosfomycin disodium",
      "labeler_name": "Meitheal Pharmaceuticals Inc.",
      "brand_name": "Contepo",
      "active_ingredients": [
        {
          "name": "FOSFOMYCIN SODIUM",
          "strength": "6 g/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "71288-035-52",
          "description": "12 VIAL, GLASS in 1 CARTON (71288-035-52)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (71288-035-51)",
          "marketing_start_date": "20251022",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Meitheal Pharmaceuticals Inc."
        ],
        "rxcui": [
          "2725577",
          "2725582"
        ],
        "spl_set_id": [
          "855574f2-39f8-43bc-a3d2-79dbb578cb94"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "97MMO19FNO"
        ]
      },
      "marketing_category": "NDA",
      "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
      "spl_id": "ab03fd88-8988-4165-ab2a-48a5da12c7ba",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "INTRAVENOUS"
      ],
      "marketing_start_date": "20251022",
      "product_id": "71288-035_ab03fd88-8988-4165-ab2a-48a5da12c7ba",
      "application_number": "NDA212271",
      "brand_name_base": "Contepo"
    }
  ]
}