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AIMOVIG

Active substance: erenumab

INJECTION · ERENUMAB 70 mg/mL

United StatesActive

Marketing holder: Amgen, 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
  • Aimovig
    erenumab
    EMEA/H/C/004447
    Novartis Europharm Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-783f-7a36-ae73-70ccb0d8d04a,01a12093-c3d7-72be-89f9-e73e6ff6b55f,01a12093-c4ed-78b1-90a8-8370c772c667,01a12096-450e-73da-b759-f6376eabeb50;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
55513-841
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 55513-841 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 55513-841 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 55513-841 · Verified 2026-10-09 · open in source