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VEOZAH

Active substance: fezolinetant

TABLET, FILM COATED · FEZOLINETANT 45 mg/1

United StatesActive

Marketing holder: Astellas Pharma US, 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
  • Veoza
    fezolinetant
    EMEA/H/C/005851
    Astellas Pharma Europe B.V.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12095-0fc3-7d5a-a467-59ceb76e614c,01a12099-ad53-719a-8840-d1a1356e8725,01a12099-ad7e-76d3-afe9-63f3e07f3c7b;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0469-2760
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0469-2760 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0469-2760 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0469-2760 · Verified 2026-10-09 · open in source