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Drugs & Devices

Rubraca

rucaparib

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Primary source: US · Source publication:
Source checked:

Rubraca · US package-label artwork; supplied packaging may differ.
US package-label artwork; supplied packaging may differ.

Clinical source excerpts are in English. Review the original label with your clinician.

What is it used for?

RUBRACA is indicated for the treatment of adult patients with a deleterious BRCAmutation (germline and/or somatic)-associated metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor-directed therapy. Select patients for therapy based on an FDA-approved companion diagnostic for RUBRACA .

Read the primary source

This source does not establish current stock, import permission or personal eligibility in China. The treating clinician and provider must confirm these separately.

Product details

Active ingredient
rucaparib
Form and strength
TABLET, FILM COATED · 200 mg; TABLET, FILM COATED · 300 mg; TABLET, FILM COATED · 250 mg
Manufacturer / applicant
PHARMAAND GMBH

Tablets (200 mg): blue, round, immediate-release, film-coated, debossed with “C2”. Tablets (250 mg): white, diamond, immediate-release, film-coated, debossed with “C25”. Tablets (300 mg): yellow, oval, immediate-release, film-coated, debossed with “C3”.

Safety and clinical review

Ask your clinician to review the complete label, medical history, other medicines, allergies, pregnancy or breastfeeding and any required monitoring. Do not start, stop or change treatment from this page.

Read the primary source

Prepare your enquiry

Include the brand or generic name, strength, dosage form, requested quantity and country where care is needed. You can attach a prescription when you continue.

Questions patients ask

What is Rubraca used for?

RUBRACA is indicated for the treatment of adult patients with a deleterious BRCAmutation (germline and/or somatic)-associated metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor-directed therapy. Select patients for therapy based on an FDA-approved companion diagnostic for RUBRACA .

This source does not establish current stock, import permission or personal eligibility in China. The treating clinician and provider must confirm these separately.

Which formulation of Rubraca should I ask about?

TABLET, FILM COATED · 200 mg; TABLET, FILM COATED · 300 mg; TABLET, FILM COATED · 250 mg

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What determines the price of Rubraca?

A current quote depends on the exact presentation, quantity, provider and access arrangements. A catalogue entry is not a stock or delivery promise. Medical charges are paid to the provider, separately from coordination fees.

What should I check before using Rubraca?

Ask your clinician to review the complete label, medical history, other medicines, allergies, pregnancy or breastfeeding and any required monitoring. Do not start, stop or change treatment from this page.

Sources and review scope

FDA prescribing information

Read the primary source

RUBRACA (RUCAPARIB) TABLET, FILM COATED [PHARMAAND GMBH]

Primary source: US · Source publication:
Source checked:

This source does not establish current stock, import permission or personal eligibility in China. The treating clinician and provider must confirm these separately.

More catalogue entries

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