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PADCEV EJFV

Active substance: enfortumab vedotin

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · ENFORTUMAB VEDOTIN 20 mg/2mL

United StatesActive

Marketing holder: SEAGEN 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 1
  • Падцев Онко
    лиофилизат для приготовления концентрата для приготовления раствора для инфузий, 20 мг, 20 мг (original in Russian, GRLS)
    ЛП-№(002568)-(РГ-RU)
    Астеллас Фарма Юроп Б.В.
EU 1
  • Padcev
    Enfortumab vedotin
    EMEA/H/C/005392
    Astellas Pharma Europe B.V.
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-4a9f-7664-a7a3-9dfa5bc662d8;count=1 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-6d64-7819-add8-fa4d5c3a2626,01a1208d-3496-79e6-bb75-487741389238;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
51144-020
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 51144-020 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 51144-020 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 51144-020 · Verified 2026-10-09 · open in source