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Iclusig

Active substance: ponatinib

TABLET, FILM COATED · PONATINIB HYDROCHLORIDE 45 mg/1

United StatesActive

Marketing holder: Takeda Pharmaceuticals America, 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
  • Iclusig
    ponatinib
    EMEA/H/C/002695
    Incyte Biosciences Distribution B.V.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-8b7b-787e-b70f-97baa91a39c5,01a1208e-a07b-7755-9e10-05e69f87c6a9,01a12098-f92f-7c3b-84cf-1d8a326340a0,01a1209b-7e03-7104-9d4b-1104ff640d10;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
63020-534
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 63020-534 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 63020-534 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 63020-534 · Verified 2026-10-09 · open in source