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LUMAKRAS

Active substance: sotorasib

TABLET, COATED · SOTORASIB 240 mg/1

United StatesActive

Marketing holder: Amgen 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
  • Lumykras
    sotorasib
    EMEA/H/C/005522
    Amgen Europe B.V.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208e-7a30-727a-bb7f-a6b0ab8c6969,01a1209b-3c9e-79cc-acdb-c948c102bb08,01a1209d-8ce1-7cd4-a4aa-e642798368ae;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
55513-512
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 55513-512 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 55513-512 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 55513-512 · Verified 2026-10-09 · open in source