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Levitra

Active substance: vardenafil

vardenafil

Centralised EU authorisationActive

Marketing holder: Bayer AG 

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 6
  • Варденафил Канон
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-№(008148)-(РГ-RU)
    Закрытое акционерное общество "Канонфарма продакшн" (ЗАО "Канонфарма продакшн")
  • Варденафил Канон
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-007687
    Закрытое акционерное общество "Канонфарма продакшн" (ЗАО "Канонфарма продакшн")
  • Варденафил-Акрихин
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-005321
    Фармацевтический завод "ПОЛЬФАРМА" АО
  • Левитра®
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-№(000297)-(РГ-RU)
    Байер АГ
  • Левитра®
    таблетки покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    П N015037/01
    Байер АГ
All products in this country (6)
US 43
  • VARDENAFIL
    TABLET, FILM COATED · VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1
    70710-1068
    Zydus Pharmaceuticals USA Inc.
  • VARDENAFIL
    TABLET, FILM COATED · VARDENAFIL HYDROCHLORIDE TRIHYDRATE 5 mg/1
    70710-1069
    Zydus Pharmaceuticals USA Inc.
  • VARDENAFIL
    TABLET, FILM COATED · VARDENAFIL HYDROCHLORIDE TRIHYDRATE 5 mg/1
    70771-1048
    Zydus Lifesciences Limited
  • VARDENAFIL
    TABLET, FILM COATED · VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1
    70771-1050
    Zydus Lifesciences Limited
  • VARDENAFIL
    TABLET, FILM COATED · VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1
    70771-1049
    Zydus Lifesciences Limited
All products in this country (43)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-9242-7acf-9085-5914e7d0dae9,01a120c4-b48a-742d-9d1c-031b143a72d2,01a120c4-bacd-7b33-a1dd-b19503334d8e,01a120c5-2773-7984-8b42-1013ee4391fa,01a120c5-8c93-7606-8b17-1b7ede34a096;count=6 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2b71-739e-8ebb-3458d1ba68cb,01a1208c-2b73-7b9d-a716-2c7be8581346,01a1208c-59d3-79b2-9dda-5eeb6d56e9dd,01a1208c-59d5-7238-a9b6-69283eb5e0a6,01a1208c-6241-7126-9977-e7a9f12606d7;count=43 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/000475
Registration status
Active
ATC code
G04BE09
Sources
  • product · EMA · EMEA/H/C/000475 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/000475 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/000475 · Verified 2026-10-09