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Telmisartan Actavis

Active substance: telmisartan

telmisartan

Centralised EU authorisationActive

Marketing holder: Actavis Group PTC ehf

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 67
  • АКТИТЕНЗ®
    таблетки, 5 мг+80 мг (original in Russian, GRLS)
    ЛП-№(007272)-(РГ-RU)
    Общество с ограниченной ответственностью "ПАНБИО ФАРМ"
  • Илпион®
    таблетки, 2.5 мг + 80 мг (original in Russian, GRLS)
    ЛП-№(012206)-(РГ-RU)
    Акционерное общество "ПРО.МЕД.ЦС" (АО "ПРО.МЕД.ЦС")
  • МИКАФОР
    таблетки, 12.5 мг+40 мг (original in Russian, GRLS)
    ЛП-№(004521)-(РГ-RU)
    Хайгланс Лабораториз Пвт. Лтд
  • МИКАФОР
    таблетки, 12.5 мг+40 мг (original in Russian, GRLS)
    ЛП-005462
    Хайгланс Лабораториз Пвт. Лтд
  • Микардис®
    таблетки, 40 мг (original in Russian, GRLS)
    ЛП-№(000159)-(РГ-RU)
    Берингер Ингельхайм Интернешнл ГмбХ
All products in this country (67)
US 120
  • Micardis HCT
    TABLET · TELMISARTAN 40 mg/1, HYDROCHLOROTHIAZIDE 12.5 mg/1
    0597-0043
    Boehringer Ingelheim Pharmaceuticals, Inc.
  • Micardis HCT
    TABLET · TELMISARTAN 80 mg/1, HYDROCHLOROTHIAZIDE 12.5 mg/1
    0597-0044
    Boehringer Ingelheim Pharmaceuticals, Inc.
  • Micardis HCT
    TABLET · TELMISARTAN 80 mg/1, HYDROCHLOROTHIAZIDE 25 mg/1
    0597-0042
    Boehringer Ingelheim Pharmaceuticals, Inc.
  • TELMISARTAN
    TABLET · TELMISARTAN 40 mg/1
    62135-536
    Chartwell RX, LLC.
  • TELMISARTAN
    TABLET · TELMISARTAN 20 mg/1
    62135-535
    Chartwell RX, LLC.
All products in this country (120)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-2f9d-7a44-bca8-986619b5d42c,01a120c3-2fdc-7181-ab2b-e55f4e55f04d,01a120c3-33ac-769e-bfc2-8c95a3f4f1ad,01a120c3-34eb-7c88-860f-f81bc4c9d06c,01a120c3-3984-770d-880f-819ddeefdd4d;count=27 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2cd2-745d-bd59-229aebdd0067,01a1208c-67e7-7a4e-9a16-09081ebc396c,01a1208c-9843-7e3f-bc1d-4643000e8112,01a1208c-9efb-7459-b555-70d4fec8b9ae,01a1208c-9fed-7365-93b3-9a78891cc583;count=80 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/001168
Registration status
Active
ATC code
C09CA07
Sources
  • product · EMA · EMEA/H/C/001168 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/001168 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/001168 · Verified 2026-10-09