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SPEVIGO

Active substance: spesolimab

INJECTION · SPESOLIMAB 300 mg/1

United StatesActive

Marketing holder: Boehringer Ingelheim Pharmaceuticals, 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
  • Spevigo
    spesolimab
    EMEA/H/C/005874
    LEO Pharma A/S
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-326f-7104-a164-8b88a2e7cb3e,01a1208c-32b3-7c03-9730-ba1eae7d6b58,01a1208d-2ee6-75e4-aaef-0998e54ee0bf,01a1208f-1d23-7dc2-bf9c-61b4add100ed,01a12093-92ce-74d0-96e3-9b1562efa03e;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0597-7705
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 0597-7705 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0597-7705 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0597-7705 · Verified 2026-10-09 · open in source