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WELIREG

Active substance: belzutifan

TABLET, FILM COATED · BELZUTIFAN 40 mg/1

United StatesActive

Marketing holder: Merck Sharp & Dohme LLC

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
  • Welireg
    belzutifan
    EMEA/H/C/005636
    Merck Sharp & Dohme B.V.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12098-5bcd-7970-a59e-c78196928bfd;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0006-5331
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0006-5331 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0006-5331 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0006-5331 · Verified 2026-10-09 · open in source