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BRIUMVI

Active substance: ublituximab

INJECTION, SOLUTION, CONCENTRATE · UBLITUXIMAB 150 mg/6mL

United StatesActive

Marketing holder: TG Therapeutics, 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
  • Briumvi
    ublituximab
    EMEA/H/C/005914
    Neuraxpharm Pharmaceuticals S.L.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1209c-1a0c-7364-b1d0-e8f1d235e8e5;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
73150-150
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 73150-150 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 73150-150 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 73150-150 · Verified 2026-10-09 · open in source