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Bimzelx

Active substance: bimekizumab

INJECTION, SOLUTION · BIMEKIZUMAB 320 mg/2mL

United StatesActive

Marketing holder: UCB, 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
EU 1
  • Bimzelx
    bimekizumab
    EMEA/H/C/005316
    UCB Pharma S.A.  
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208e-6160-77fc-b2c3-f2576ce16f52,01a1208e-6165-7c3e-bf8f-10ddbfa5f433,01a12096-047b-7271-84df-199f9f2fa52c,01a1209b-1193-7b7a-ae82-f2cf7f47b177;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50474-783
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 50474-783 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50474-783 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50474-783 · Verified 2026-10-09 · open in source