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Rubraca

Active substance: rucaparib camsylate

rucaparib camsylate

Centralised EU authorisationActive

Marketing holder: pharmaand GmbH

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 3
  • Rubraca
    TABLET, FILM COATED · RUCAPARIB CAMSYLATE 200 mg/1
    82154-0783
    pharmaand GmbH
  • Rubraca
    TABLET, FILM COATED · RUCAPARIB CAMSYLATE 300 mg/1
    82154-0785
    pharmaand GmbH
  • Rubraca
    TABLET, FILM COATED · RUCAPARIB CAMSYLATE 250 mg/1
    82154-0784
    pharmaand GmbH
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12091-138e-7924-b0b6-d36f2c0b4373,01a12091-1393-77ca-ab65-4832a8e01e1c,01a12095-311b-7dc4-89ed-cf07cc0e8964;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/004272
Registration status
Active
ATC code
L01XX
Sources
  • product · EMA · EMEA/H/C/004272 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/004272 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/004272 · Verified 2026-10-09