Venlafaxine SUN 150 mg, tabletten met verlengde afgifte

{
  "form": "Tablet met verlengde afgifte",
  "route": "Oraal gebruik",
  "soort": "RVG",
  "source": "cbg_meb",
  "smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h105066_smpc.pdf",
  "strength": null,
  "atc_label": "Venlafaxine",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg105066",
  "excipients": [
    "ALLURAROOD AC ALUMINIUM LAK (E 129)",
    "CELLULOSE, MICROKRISTALLIJN (E 460(i))",
    "COPOLYMEER VAN ETHYLACRYLAAT-METHACRYLZUUR (1:1)",
    "CROSPOVIDON (E 1202)",
    "DIBUTYLSEBACAAT",
    "ETHYLCELLULOSE (E 462)",
    "HYPROMELLOSE (Release controlling polymer)(E 464)",
    "IJZEROXIDE ZWART (E 172)",
    "LACTOSE 1-WATER",
    "MACROGOL 3350",
    "MAGNESIUMSTEARAAT (E 470b)",
    "MAGNESIUMSTEARAAT (E 470b)",
    "MANNITOL (D-) (E 421)",
    "NATRIUMLAURILSULFAAT",
    "POLYSORBAAT 20 (E 432)",
    "POLYSORBAAT 80 (E 433)",
    "POLYVINYLALCOHOL, GEDEELTELIJK GEHYDROLYSEERD (E1203)",
    "POVIDON K 30 (E 1201)",
    "POVIDON K 30 (E 1201)",
    "PROPYLEENGLYCOL (E 1520)",
    "SCHELLAK GLAZE, GEDEELTELIJK VERESTERD",
    "SILICIUMDIOXIDE (E 551)",
    "TALK (E 553b)",
    "TALK (E 553b)",
    "TALK (E 553b)",
    "TRIETHYLCITRAAT (E 1505)",
    "ZWARTE INKT"
  ],
  "substances": [
    "VENLAFAXINEHYDROCHLORIDE"
  ],
  "leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h105066.pdf",
  "authorised_at": "2010/12/14",
  "procedure_number": "NL/H/3948/003",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "105066",
  "additional_monitoring": "N"
}