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KISQALI

Active substance: ribociclib

TABLET, FILM COATED · RIBOCICLIB SUCCINATE 200 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
  • Kisqali
    ribociclib succinate
    EMEA/H/C/004213
    Novartis Europharm Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-fa83-7c19-b808-0465b46915cf,01a1208c-fa89-7c20-aecd-3d20fead3591,01a1208e-0331-79e6-bd75-b849d1f5ce2a;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0078-0874
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0078-0874 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0078-0874 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0078-0874 · Verified 2026-10-09 · open in source