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Isturisa

Active substance: osilodrostat

osilodrostat phosphate

Centralised EU authorisationActive

Marketing holder: Recordati Rare Diseases

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 4
  • Isturisa
    TABLET, COATED · OSILODROSTAT PHOSPHATE 1 mg/1
    55292-330
    Recordati Rare Diseases, Inc.
  • Isturisa
    TABLET, COATED · OSILODROSTAT PHOSPHATE 5 mg/1
    55292-331
    Recordati Rare Diseases, Inc.
  • Isturisa
    TABLET, COATED · OSILODROSTAT PHOSPHATE 5 mg/1
    55292-321
    Recordati Rare Diseases, Inc.
  • Isturisa
    TABLET, COATED · OSILODROSTAT PHOSPHATE 1 mg/1
    55292-320
    Recordati Rare Diseases, Inc.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-77c3-7718-ada5-0cab6dc73e96,01a1208d-4380-7ccd-b0e1-08f30629f79a,01a1208e-78fe-7199-9e92-aff2d5ebffb5,01a12093-c0d4-77dd-a593-f4154193a278;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/004821
Registration status
Active
ATC code
H02CA02
Sources
  • product · EMA · EMEA/H/C/004821 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/004821 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/004821 · Verified 2026-10-09