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TEZSPIRE

Active substance: tezepelumab

INJECTION, SOLUTION · TEZEPELUMAB 210 mg/1.9mL

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
  • Tezspire
    tezepelumab
    EMEA/H/C/005588
    AstraZeneca AB
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12093-c3b5-7c78-8e1d-eea4a3c4da95,01a1209d-8cd1-7b3a-a70c-c0ae8d47996f;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
55513-123
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 55513-123 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 55513-123 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 55513-123 · Verified 2026-10-09 · open in source