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ACTEMRA

Active substance: tocilizumab

INJECTION, SOLUTION, CONCENTRATE · TOCILIZUMAB 80 mg/4mL

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 6
  • Актемра®
    раствор для подкожного введения, 162 мг/0.9 мл, 0.9 мл (original in Russian, GRLS)
    ЛП-003186
    Ф. Хоффманн-Ля Рош Лтд.
  • Актемра®
    раствор для подкожного введения, 162 мг, 0.9 мл (original in Russian, GRLS)
    ЛП-№(004451)-(РГ-RU)
    Ф.Хоффманн-Ля Рош Лтд
  • Актемра®
    концентрат для приготовления раствора для инфузий, 20 мг/мл, 20 мл (original in Russian, GRLS)
    ЛП-№(005225)-(РГ-RU)
    Ф.Хоффманн-Ля Рош Лтд
  • Актемра®
    концентрат для приготовления раствора для инфузий, 20 мг/мл, 20 мл (original in Russian, GRLS)
    ЛСР-003012/09
    Ф. Хоффманн-Ля Рош Лтд.
  • Компларейт®
    концентрат для приготовления раствора для инфузий, 20 мг/мл, 10 мл (original in Russian, GRLS)
    ЛП-№(006657)-(РГ-RU)
    Акционерное общество "ГЕНЕРИУМ" (АО "ГЕНЕРИУМ")
All products in this country (6)
EU 5
  • Avtozma
    tocilizumab
    EMEA/H/C/006196
    Celltrion Healthcare Hungary Kft.
  • RoActemra
    tocilizumab
    EMEA/H/C/000955
    Roche Registration GmbH
  • Tocilizumab STADA (previously Tofidence)
    tocilizumab
    EMEA/H/C/005984
    STADA Arzneimittel AG
  • Tuyory
    tocilizumab
    EMEA/H/C/006416
    Chemical Works of Gedeon Richter Plc. (Gedeon Richter Plc.)
  • Tyenne
    tocilizumab
    EMEA/H/C/005781
    Fresenius Kabi Deutschland GmbH
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-2e90-7840-bb17-91291b260e6a,01a120c3-610f-7235-b903-1efb61877d9a,01a120c3-6a2c-71ff-9ce6-de8578e005cd,01a120c3-7e4c-7a8f-a52a-c2c5736f6aec,01a120c3-c922-7571-a3a4-de57100f2827;count=6 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2cdf-7eb5-9033-5b585f91742c,01a1208c-959c-7143-b2bf-7a9efe98a1df,01a1208c-98bb-7cc2-be54-f8b8995c1ed0,01a1208d-3064-789a-a2cb-baa5452e9cea,01a1208d-3067-7bed-9bfe-3e27a0a8d4dd;count=22 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50242-135
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 50242-135 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50242-135 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50242-135 · Verified 2026-10-09 · open in source