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FASENRA

Active substance: benralizumab

INJECTION, SOLUTION · BENRALIZUMAB 10 mg/.5mL

United StatesActive

Marketing holder: AstraZeneca Pharmaceuticals LP

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
  • Fasenra
    Benralizumab
    EMEA/H/C/004433
    AstraZeneca AB
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-9502-7d85-8a3e-cd216986eb95,01a1208d-7179-7969-a099-c3157b97e64a,01a1208f-8223-78eb-a52b-03316756d1fa,01a12092-4328-7970-94e1-32119742acdb;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0310-1745
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 0310-1745 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0310-1745 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0310-1745 · Verified 2026-10-09 · open in source