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Columvi

Active substance: glofitamab

SOLUTION, CONCENTRATE · GLOFITAMAB 2.5 mg/2.5mL

United StatesActive

Marketing holder: Genentech, 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
  • Columvi
    Glofitamab
    EMEA/H/C/005751
    Roche Registration GmbH 
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208e-6009-7999-8671-223d4d7f0822,01a12098-bc20-777d-ad30-0abbeab960c7;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50242-125
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 50242-125 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50242-125 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50242-125 · Verified 2026-10-09 · open in source