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Nucala

Active substance: mepolizumab

INJECTION, SOLUTION · MEPOLIZUMAB 40 mg/.4mL

United StatesActive

Marketing holder: GlaxoSmithKline LLC

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 3
  • Нукала
    раствор для подкожного введения, 100 мг/мл, 1 мл (original in Russian, GRLS)
    ЛП-№(001771)-(РГ-RU)
    АО "ГлаксоСмитКляйн Трейдинг"
  • Нукала
    лиофилизат для приготовления раствора для подкожного введения, 100 мг, 100 мг (original in Russian, GRLS)
    ЛП-№(012190)-(РГ-RU)
    АО "ГлаксоСмитКляйн Трейдинг"
  • Нукала
    лиофилизат для приготовления раствора для подкожного введения, 100 мг, 100 мг (original in Russian, GRLS)
    ЛП-004794
    АО "ГлаксоСмитКляйн Трейдинг"
EU 2
  • Bosatria
    Mepolizumab
    EMEA/H/C/001069
    Glaxo Group Limited
  • Nucala
    Mepolizumab
    EMEA/H/C/003860
    GlaxoSmithKline Trading Services Limited
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-430e-7482-95a5-c73f4e6c2610,01a120c3-ca43-78f4-9d54-1174fcc90d38,01a120c5-c55a-7ab0-a658-7ea8f7cf5998;count=3 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-5e93-7f58-bb4b-dac1adb409e4,01a1208c-5ea3-75eb-afad-6fe8cad3955f,01a12091-9793-7eb0-b5ae-fd0c1778dad4;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0173-0904
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 0173-0904 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0173-0904 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0173-0904 · Verified 2026-10-09 · open in source