Active ingredient
Rucaparib
3 finished FDA listings contain Rucaparib as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- RUCAPARIB CAMSYLATE
- Dosage forms
- Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 1
- Strengths listed
- 200 mg/1 · 250 mg/1 · 300 mg/1
- Brand names in FDA listings
- Rubraca
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 1862579
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| NDA 209115 | PHARMAAND | 2016-12-19 | 3 |
Official labeling on DailyMed
- RUBRACA (RUCAPARIB) TABLET, FILM COATED [PHARMAAND GMBH] · version 19 · 2026-01-02
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.