{
  "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": "2026-10-13",
    "results": {
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      "generic_name": "Copper",
      "labeler_name": "Organon LLC",
      "brand_name": "Miudella",
      "active_ingredients": [
        {
          "name": "COPPER",
          "strength": "175 mm/1"
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      "finished": true,
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          "description": "1 TRAY in 1 BOX, UNIT-DOSE (78206-210-01)  / 1 INTRAUTERINE DEVICE in 1 TRAY",
          "marketing_start_date": "20251201",
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        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
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        ],
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          "Copper [CS]"
        ],
        "pharm_class_epc": [
          "Copper-containing Intrauterine Device [EPC]"
        ],
        "pharm_class_pe": [
          "Decreased Embryonic Implantation [PE]",
          "Decreased Sperm Motility [PE]",
          "Inhibit Ovum Fertilization [PE]"
        ],
        "unii": [
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      },
      "marketing_category": "NDA",
      "dosage_form": "INTRAUTERINE DEVICE",
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      "application_number": "NDA218201",
      "brand_name_base": "Miudella",
      "pharm_class": [
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        "Copper-containing Intrauterine Device [EPC]",
        "Decreased Embryonic Implantation [PE]",
        "Decreased Sperm Motility [PE]",
        "Inhibit Ovum Fertilization [PE]"
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}