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Amvuttra

Active substance: vutrisiran

vutrisiran sodium

Centralised EU authorisationActive

Marketing holder: Alnylam Netherlands B.V.

Verified 2026-10-09 · EMA

Analogues in other countries
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 1
  • AMVUTTRA
    INJECTION · VUTRISIRAN SODIUM 25 mg/.5mL
    71336-1003
    Alnylam Pharmaceuticals, Inc.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-c620-7a23-a807-d9fcd72fae4f;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/005852
Registration status
Active
ATC code
N07XX18
Sources
  • product · EMA · EMEA/H/C/005852 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/005852 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/005852 · Verified 2026-10-09