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Augtyro

Active substance: repotrectinib

CAPSULE · REPOTRECTINIB 40 mg/1

United StatesActive

Marketing holder: E.R. Squibb & Sons, L.L.C.

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
  • Augtyro
    repotrectinib
    EMEA/H/C/006005
    Bristol-Myers Squibb Pharma EEIG
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12095-823f-79db-a907-ff3bb58e2ac0,01a1209a-c7bc-7576-b6c9-2ac76cedfde6;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0003-4040
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0003-4040 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0003-4040 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0003-4040 · Verified 2026-10-09 · open in source