rucaparib camsylate · Pharmaand · NDA 209115

Rubraca

Earliest generic entry, as listed · earliest of 3 marketed strengths
17 Aug 2035

Blocked by patent: US 10130636, US 10130636, US 10130636, US 10130636, US 9987285.

Listed patents · 19 unexpired

PatentClaimsExpires
US 10130636use U-283017 Aug 2035
US 10130636use U-227317 Aug 2035
US 10130636use U-210117 Aug 2035
US 10130636use U-201217 Aug 2035
US 9987285product17 Aug 2035
US 8859562use U-20124 Aug 2031
US 8859562use U-22734 Aug 2031
US 8859562use U-28304 Aug 2031
US 10278974product10 Feb 2031
US 8754072substance, product10 Feb 2031
US 9045487substance, product10 Feb 2031
US 9861638use U-227310 Feb 2031
US 9861638use U-201210 Feb 2031
US 8071579use U-201212 Aug 2027
US 8071579use U-227312 Aug 2027
US 8071579use U-283012 Aug 2027
US 8143241use U-201212 Aug 2027
US 8143241use U-283012 Aug 2027
US 8143241use U-227312 Aug 2027

Exclusivities · 1 unexpired

I-982new indication (3 years)17 Dec 2028

Paragraph IV certifications · 0

No Paragraph IV certification listed by FDA for this drug.

The list shows that a generic applicant certified to FDA that a listed patent is invalid or not infringed. It does not show litigation, settlements or launch timing.

Event history

No events yet. The first ingestion only records products entering their 12-month window; changes appear from the next Orange Book update.

Products covered · 3

NDA · productFormStrengthListed expiry
209115 · 001 · RLDtablet, oralEQ 200MG BASE17 Aug 2035
209115 · 002 · RLDtablet, oralEQ 300MG BASE17 Aug 2035
209115 · 003 · RLDtablet, oralEQ 250MG BASE17 Aug 2035