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ZELBORAF

Active substance: vemurafenib

TABLET, FILM COATED · VEMURAFENIB 240 mg/1

United StatesActive

Marketing holder: Genentech, Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
RU 2
  • Зелбораф®
    таблетки, покрытые пленочной оболочкой, 240 мг (original in Russian, GRLS)
    ЛП-№(000249)-(РГ-RU)
    Ф.Хоффманн-Ля Рош Лтд
  • Зелбораф®
    таблетки, покрытые пленочной оболочкой, 240 мг (original in Russian, GRLS)
    ЛП-002271
    Ф. Хоффманн-Ля Рош Лтд.
EU 1
  • Zelboraf
    vemurafenib
    EMEA/H/C/002409
    Roche Registration GmbH
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-353f-7908-ad81-91ab6027763f,01a120c5-0d30-7b24-a6ca-3c2b73c323dc;count=2 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a12096-00b8-7bdf-9f85-71cc4040e466;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50242-090
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 50242-090 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50242-090 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50242-090 · Verified 2026-10-09 · open in source