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KRAZATI

Active substance: adagrasib

TABLET, COATED · ADAGRASIB 200 mg/1

United StatesActive

Marketing holder: Mirati Therapeutics, 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
  • Krazati
    adagrasib
    EMEA/H/C/006013
    Bristol-Myers Squibb Pharma EEIG
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208f-26ae-759e-8b71-579d26e6513e;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
80739-812
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 80739-812 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 80739-812 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 80739-812 · Verified 2026-10-09 · open in source