pillbase.ru

Ocrevus

Active substance: ocrelizumab

ocrelizumab

Centralised EU authorisationActive

Marketing holder: Roche Registration GmbH

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
RU 3
  • Окревус®
    концентрат для приготовления раствора для инфузий, 30 мг/мл, 10 мл (original in Russian, GRLS)
    ЛП-004503
    Ф. Хоффманн-Ля Рош Лтд.
  • Окревус®
    концентрат для приготовления раствора для инфузий, 300 мг, 10 мл (original in Russian, GRLS)
    ЛП-№(003473)-(РГ-RU)
    Ф.Хоффманн-Ля Рош Лтд
  • Окревус®
    раствор для подкожного введения, 920 мг, 23 мл (original in Russian, GRLS)
    ЛП-№(016128)-(РГ-RU)
    Ф.Хоффманн-Ля Рош Лтд
US 2
  • OCREVUS
    INJECTION · OCRELIZUMAB 300 mg/10mL
    50242-150
    Genentech, Inc.
  • Ocrevus Zunovo
    INJECTION, SOLUTION · OCRELIZUMAB 920 mg/23mL, HYALURONIDASE (HUMAN RECOMBINANT) 23000 U/23mL
    50242-554
    Genentech, Inc.
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-2fe9-7ae6-85e4-405dc5672986,01a120c3-54c3-7a50-8af2-77bb45290e15,01a120c3-f8c5-7032-920a-c4d592f8b263;count=3 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a12093-93bf-762b-9927-493f2dcd6314;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/004043
Registration status
Active
ATC code
L04AG08
Sources
  • product · EMA · EMEA/H/C/004043 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/004043 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/004043 · Verified 2026-10-09