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Product profile · United States

RUBRACA

 ·  Patent Litigation & Settlement History ↓

IngredientRUCAPARIB CAMSYLATE
Application typeNDA
Application209115
Product003
Dosage formTABLET
RouteORAL
StrengthEQ 250MG BASE
Approval date2017-05-01
Marketing statusPrescription
Status event—
ApplicantPHARMAAND
Product source

Current GenericRadar decision

Year2031
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typePATENT
Anchor date2031-02-10
Patent anchor2031-02-10
Exclusivity anchor2021-12-19
Protection date2035-08-17
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_EXIST; US:NDA:209115:003; exact Final ANDA not verified; not proof of generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
80715792027-08-12U U-2012NNU
English description not available.
———
80715792027-08-12U U-2830NNU
English description not available.
———
80715792027-08-12U U-2273NNU
English description not available.
———
80715792027-08-12ORANGE_BOOK U-2012,U-2273,U-2830NNU
English description not available.
———
81432412027-08-12U U-2012NNU
English description not available.
———
81432412027-08-12U U-2273NNU
English description not available.
———
81432412027-08-12U U-2830NNU
English description not available.
———
81432412027-08-12ORANGE_BOOK U-2012,U-2273,U-2830NNU
English description not available.
———
102789742031-02-10DP —NNDP
English description not available.
———
102789742031-02-10ORANGE_BOOK —NNDP
English description not available.
———
87540722031-02-10DS/DP —NNDP
English description not available.
———
87540722031-02-10ORANGE_BOOK —NNDP
English description not available.
———
90454872031-02-10DS/DP —NYU
English description not available.
———
90454872031-02-10ORANGE_BOOK —NYU
English description not available.
———
98616382031-02-10U U-2012NNU
English description not available.
———
98616382031-02-10U U-2273NNU
English description not available.
———
98616382031-02-10ORANGE_BOOK U-2012,U-2273NNU
English description not available.
———
88595622031-08-04U U-2830NNU
English description not available.
———
88595622031-08-04U U-2273NNU
English description not available.
———
88595622031-08-04U U-2012NNU
English description not available.
———
88595622031-08-04ORANGE_BOOK U-2012,U-2273,U-2830NNU
English description not available.
———
101306362035-08-17U U-2830NNU
English description not available.
———
101306362035-08-17U U-2012NNU
English description not available.
———
101306362035-08-17U U-2101NNU
English description not available.
———
101306362035-08-17U U-2273NNU
English description not available.
———
101306362035-08-17ORANGE_BOOK U-2012,U-2101,U-2273,U-2830NNU
English description not available.
———
99872852035-08-17DP —NNDP
English description not available.
———
99872852035-08-17ORANGE_BOOK —NNDP
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
I-7722018-04-062021-04-06English description not available.NN—
NCE
Full coverage date: —
Source
NCE2016-12-192021-12-19English description not available.YY2021-12-19
NCE
Full coverage date: 2021-12-19
Source
ODE-1262016-12-192022-06-10English description not available.NN—
NCE
Full coverage date: —
Source
I-8302020-05-152023-05-15English description not available.NN—
NCE
Full coverage date: —
Source
ODE-1682018-04-062025-04-06English description not available.NN—
NCE
Full coverage date: —
Source
I-9822025-12-172028-12-17English description not available.NN——Source
I-9822025-12-172028-12-17English description not available.NN—
NCE
Full coverage date: —
Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

Market Entry Information

API filings, authorized generics and linked regulatory milestones.

API Master Files & Certifications 0 records

Ingredient-level registrations from linked public manufacturer portfolios. A filing does not establish supply to this finished product. DMFs are not FDA approvals.

APIHolder / manufacturerHolder countryFiling typeNumberStatusFiled dateAvailable for referenceSourceLast verified
No master-file or certification records are linked through public manufacturer portfolios.

Authorized Generics 0 records

Authorized generics are shown separately from independent ANDA approvals.

Application / productApplicantEvent / status First marketed Product mappingSourceLast verified
No authorized-generic records are linked to this product.

Tentative ANDA Approvals 0 records

Tentative approval is not final approval. Historical tentative approvals remain visible after a linked final approval.

Application / productApplicantEvent / status Tentative date Follow-up final approvalProduct mappingSourceLast verified
No tentative-approval records are linked to this product.

Paragraph IV Challenges 0 records

Paragraph IV challenges below are sourced from legal records separately from FDA approvals. An ANDA filing, lawsuit or settlement does not establish final approval or commercial launch.

Application / productApplicantEvent / status Certification event date Product mappingSourceLast verified
No structured Paragraph IV certification events are linked in the available approval evidence.

Final ANDA Approvals 0 records

Approval dates do not establish commercial launch. Product mapping is shown for each linked record.

Application / productApplicantEvent / status Final approval date Product mappingSourceLast verified
No final-approval records are linked to this product.
Decision evidence (16)
TypeDateRoleBasisSource
PATENT2027-08-12HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2027-08-12HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2031-02-10HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2031-02-10HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2031-02-10CANONICAL_ANCHOREnglish description not available.Source
PATENT2031-02-10HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2031-08-04FTO_TAILEnglish description not available.Source
PATENT2035-08-17FTO_TAILEnglish description not available.Source
PATENT2035-08-17FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_STATUS2031-02-10CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_EXIST; US:NDA:209115:003; exact Final ANDA not verified; not proof of generic absenceSource
Independent legal-event information

Litigation & Settlement History

Settlement launch rights generally apply only to the named parties and product scope. These records do not change GenericRadar patent/exclusivity anchors or current decisions.

No litigation or settlement record currently linked to this product.