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EBGLYSS

Active substance: lebrikizumab

INJECTION, SOLUTION · LEBRIKIZUMAB 250 mg/2mL

United StatesActive

Marketing holder: Eli Lilly and Company

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
EU 1
  • Ebglyss
    Lebrikizumab
    EMEA/H/C/005894
    Almirall, S.A.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12091-6792-78d2-8ad3-dde7c0f59b5d,01a12095-663f-7edc-9127-54b4006a0928;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0002-7772
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 0002-7772 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0002-7772 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0002-7772 · Verified 2026-10-09 · open in source