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TUKYSA

Active substance: tucatinib

TABLET · TUCATINIB 150 mg/1

United StatesActive

Marketing holder: SEAGEN 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
  • Tukysa
    tucatinib
    EMEA/H/C/005263
    Pfizer Europe MA EEIG
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208f-d0bc-773c-ae9a-7fffbef3eee5,01a1209d-7275-7a22-9c2a-0a044497b4bb;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
51144-002
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 51144-002 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 51144-002 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 51144-002 · Verified 2026-10-09 · open in source