Neupro 2 mg/24 h pleister voor transdermaal gebruik

{
  "form": "Pleister voor transdermaal gebruik",
  "route": "Transdermaal gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/neupro-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Rotigotine",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp72669",
  "excipients": [
    "ALUMINIUMHYDROXIDE 0-WATER",
    "ASCORBYLPALMITAAT (E 304)",
    "BEIGE INKT",
    "COPOLYMEER VAN ETHYLACRYLAAT-2-ETHYLHEXYLACRYLAAT",
    "COPOLYMEER VAN POLY(DIMETHYLSILOXAAN-HYDROXIDE)(19,9)-TRIMETHYLSILYLSILICAATHARS(43,5)-HEXAMETHYLDISILAZAAN(9,9)",
    "COPOLYMEER VAN POLY(DIMETHYLSILOXAAN-HYDROXIDE)(22,6)-TRIMETHYLSILYLSILICAATHARS(38,6)-HEXAMETHYLDISILAZAAN(11,3)",
    "EPOXYHARS",
    "EPOXYHARS",
    "NATRIUMMETABISULFIET (E 223)",
    "PIGMENT GEEL 95",
    "PIGMENT GEEL 95",
    "PIGMENT ROOD 144",
    "PIGMENT ROOD 166",
    "PIGMENT ZWART 7",
    "POLYAMINOAMIDE HARS",
    "POLYAMINOAMIDE HARS",
    "POLYETHYLEENTEREPHTHALAAT, GEFLUORIDEERD",
    "POLYETHYLEENTEREPHTHALAAT, GESILICONEERD EN BEKLEED MET ALUMINIUM",
    "POLYPROPYLEEN",
    "POLYPROPYLEEN",
    "POVIDON K 90 (E 1201)",
    "SILICIUMDIOXIDE (E 551)",
    "TITAANDIOXIDE (E 171)",
    "TOCOFEROL, DL-ALFA (E 307)"
  ],
  "substances": [
    "ROTIGOTINE"
  ],
  "leaflet_url": null,
  "authorised_at": "2006/02/15",
  "procedure_number": "EMEA/H/C/000626",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/05/331",
  "additional_monitoring": "N"
}