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Hemlibra

Active substance: emicizumab

INJECTION, SOLUTION · EMICIZUMAB 12 mg/.4mL

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
  • Hemlibra
    emicizumab
    EMEA/H/C/004406
    Roche Registration Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-6ad0-7618-a507-67d572b247d1,01a1208c-6ad2-73b8-8f08-0c37f3dc9ded,01a12091-b67b-7804-9889-9c48ea153690,01a12093-93c7-7c79-a827-b5d7768f6f11,01a1209d-6da5-74ef-a26e-e2ee84cb522d;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
50242-927
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 50242-927 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 50242-927 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 50242-927 · Verified 2026-10-09 · open in source