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ZILBRYSQ

Active substance: zilucoplan

INJECTION, SOLUTION · ZILUCOPLAN 40 mg/mL

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
  • Zilbrysq
    zilucoplan
    EMEA/H/C/005450
    UCB Pharma S.A.  
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208d-31b6-73d1-acf6-9f57fb04f607,01a12096-0496-7c61-8bc9-fa33aca82e02,01a12098-bdb5-7994-ae0a-bbc52c0cbf7e;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50474-990
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 50474-990 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50474-990 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50474-990 · Verified 2026-10-09 · open in source