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Product profile · United States

VITEKTA

 ·  Patent Litigation & Settlement History ↓

IngredientELVITEGRAVIR
Application typeNDA
Application203093
Product001
Dosage formTABLET
RouteORAL
Strength85MG
Approval date2014-09-24
Marketing statusDISCONTINUED
Status event—
ApplicantGILEAD SCIENCES INC
Product source

Current GenericRadar decision

Year2017
SelectionDISQUALIFIED
ReviewFINAL
Anchor typeFDA_DISCONTINUATION
Anchor date—
Patent anchor2027-02-27
Exclusivity anchor2017-09-24
Protection date2027-04-26
First Final ANDA—
Status event—

FDA_DISCONTINUED; FDA DISC action month 2017-05

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
71762202026-08-27DS/DP/U U-257———
———
76357042026-10-26DS/DP/U U-257———
———
89811032026-10-26DS/DP ————
———
71762202027-02-27— ————
—2027-02-27—
71762202027-02-27ORANGE_BOOK U-257YNTRUE_DS
English description not available.
—2027-02-27—
76357042027-04-26— ————
—2027-04-26—
76357042027-04-26ORANGE_BOOK U-257NNDP
English description not available.
—2027-04-26—
89811032027-04-26— ————
—2027-04-26—
89811032027-04-26ORANGE_BOOK —NNDP
English description not available.
—2027-04-26—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE2012-08-272017-08-27NEW CHEMICAL ENTITYYY2017-08-27Source
NP2014-09-242017-09-24English description not available.YY2017-09-24Source

2026-10-10 · NO_RECORD_IN_CURRENT_SNAPSHOT · 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 (6)
TypeDateRoleBasisSource
PATENT2027-02-27HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2027-04-26HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2027-04-26HISTORICAL_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—HISTORICAL_CONTEXTNEW CHEMICAL ENTITYSource
REGULATORY_EXCLUSIVITY—HISTORICAL_CONTEXTEnglish description not available.Source
REGULATORY_STATUS—TERMINAL_STATUSFDA_DISCONTINUED; FDA DISC action month 2017-05Source
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.