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OXBRYTA

Active substance: voxelotor

TABLET, FILM COATED · VOXELOTOR 300 mg/1

United StatesActive

Marketing holder: Global Blood Therapeutics, Inc, A subsidiary of Pfizer 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
  • Oxbryta
    voxelotor
    EMEA/H/C/004869
    Pfizer Europe MA EEIG
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2cfa-7291-9007-f40fa474e055,01a12097-46e4-780e-ab23-f7e278899780,01a1209e-6a38-7230-bbe2-ab9f98263b96;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
72786-102
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 72786-102 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 72786-102 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 72786-102 · Verified 2026-10-09 · open in source