Lenalidomide Krka d.d. Novo mesto 10 mg, harde capsules

{
  "form": "Capsule, hard",
  "route": "Oraal gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/lenalidomide-krka-dd-novo-mesto-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Lenalidomide",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp127003",
  "excipients": [
    "CARRAGEENAN (E 407)",
    "CELLULOSE, MICROKRISTALLIJN (E 460(i))",
    "GLYCEROLDIBEHENAAT",
    "HYPROMELLOSE 2910 (3 - 15 mPa.s) (E 464)",
    "IJZEROXIDE GEEL (E 172)",
    "IJZEROXIDE ROOD  (E 172)",
    "IJZEROXIDE ZWART (E 172)",
    "INDIGOKARMIJN (E 132)",
    "KALIUMCHLORIDE (E 508)",
    "MANNITOL (D-) (E 421)",
    "MAÏSZETMEEL, GEPREGELATINEERD",
    "NATRIUMHYDROXIDE (E 524)",
    "POVIDON (E 1201)",
    "PROPYLEENGLYCOL (E 1520)",
    "SCHELLAK (E 904)",
    "TITAANDIOXIDE (E 171)",
    "TITAANDIOXIDE (E 171)",
    "WIJNSTEENZUUR, (L (+) Vorm) (E 334)",
    "WITTE INKT"
  ],
  "substances": [
    "LENALIDOMIDEHYDROCHLORIDE 1-WATER"
  ],
  "leaflet_url": null,
  "authorised_at": "2021/02/11",
  "procedure_number": "EMEA/H/C/005734",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/20/1520",
  "additional_monitoring": "N"
}