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SCEMBLIX

Active substance: asciminib

TABLET, FILM COATED · ASCIMINIB HYDROCHLORIDE 40 mg/1

United StatesActive

Marketing holder: Novartis Pharmaceuticals Corporation

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
  • Scemblix
    asciminib hydrochloride
    EMEA/H/C/005605
    Novartis Europharm Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208f-7d34-77d7-a217-0bedfa759914,01a12091-6cf4-7370-bc65-b7756875332a,01a12091-6cf9-795d-8e9d-4601100a67a1,01a12095-66b9-7ba6-9e41-7189e93079c4,01a12095-7403-7537-b1e0-95d89585289a;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0078-1098
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0078-1098 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0078-1098 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0078-1098 · Verified 2026-10-09 · open in source