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durvalumab injection, solution

Active substance: durvalumab

INJECTION, SOLUTION · DURVALUMAB 500 mg/10mL

United StatesActive

Marketing holder: Catalent Indiana, LLC

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
  • Imfinzi
    durvalumab
    EMEA/H/C/004771
    AstraZeneca AB
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208d-fc2e-7839-a3a6-9cc29356c654,01a1208f-8210-78a7-8f0a-5f40726d9a3c,01a12099-10fc-7aac-8bf8-16a7468653c9,01a1209b-8af4-73e1-b247-c04a10d26d07;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
61434-002
Registration status
Active
Dispensing
Prescription only
Sources
  • product · openFDA NDC · 61434-002 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 61434-002 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 61434-002 · Verified 2026-10-09 · open in source