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Sylvant

Active substance: siltuximab

INJECTION, POWDER, FOR SOLUTION · SILTUXIMAB 100 mg/1

United StatesActive

Marketing holder: Recordati Rare Diseases, 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
  • Sylvant
    siltuximab
    EMEA/H/C/003708
    Recordati Netherlands B.V.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12097-4edd-7f6e-a0f3-584fec3ef4a1,01a12099-dd8e-7b39-8692-b368f8fb4de9;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
73090-420
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 73090-420 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 73090-420 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 73090-420 · Verified 2026-10-09 · open in source