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Product profile · United States

BIKTARVY

 ·  Patent Litigation & Settlement History ↓

IngredientBICTEGRAVIR SODIUM; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE
Application typeNDA
Application210251
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 50MG BASE;200MG;EQ 25MG BASE
Approval date2018-02-07
Marketing statusPrescription
Status event—
ApplicantGILEAD SCIENCES INC
Product source

Current GenericRadar decision

Year2035
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2035-06-19
Patent anchor2035-06-19
Exclusivity anchor—
Protection date2036-11-08
First Final ANDA—
Status event—

GNR judgment: DEEP_REVIEW. Reference year: 2035. Anchor type: TRUE_DS_PATENT. Patent anchor: 2035-06-19. Exclusivity anchor: not recorded. Anchor date: 2035-06-19. Patent tail: yes. Exclusivity tail: no. Review status: FINAL. Historical detailed rationale is retained in the evidence snapshot; this is a structured English summary, not a literal translation.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
87540652032-08-15DS/DP/U U-257———
———
92967692032-08-15DS/DP/U U-257———
———
87540652033-02-15— ————
—2033-02-15—
87540652033-02-15ORANGE_BOOK U-257NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
—2033-02-15—
92967692033-02-15— ————
—2033-02-15—
92967692033-02-15ORANGE_BOOK U-257NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
—2033-02-15—
92169962033-12-19DS/DP ————
———
92169962033-12-19ORANGE_BOOK —YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
———
97320922033-12-19DS/DP ————
———
97320922033-12-19ORANGE_BOOK —YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
———
103850672035-06-19U U-257———
———
103850672035-06-19ORANGE_BOOK U-257NNU
Process or use limited to a particular indication, combination, regimen, population or formulation; not whole-label anchor.
———
97083422035-06-19DS/DP ————
———
97083422035-06-19ORANGE_BOOK —YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
———
105488462036-11-08DP ————
———
105488462036-11-08ORANGE_BOOK —NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
———
117448022036-11-08DP ————
———
117448022036-11-08ORANGE_BOOK —NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
———
125942442036-11-08DP/U U-257———
———
125942442036-11-08ORANGE_BOOK U-257NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-256—2026-06-18————Source
ODE-256—2026-06-18FDA posted date collected; scope not independently certified; preserved as context/tail.————Source
I-942—2027-02-23————Source
I-942—2027-02-23FDA posted date collected; scope not independently certified; preserved as context/tail.————Source
M-305—2027-04-24————Source
M-305—2027-04-24FDA posted date collected; scope not independently certified; preserved as context/tail.————Source
ODE-468—2031-02-23————Source
ODE-468—2031-02-23FDA posted date collected; scope not independently certified; preserved as context/tail.————Source
ODE-540—2032-07-30————Source
ODE-540—2032-07-30FDA posted date collected; scope not independently certified; preserved as context/tail.————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 (10)
TypeDateRoleBasisSource
PATENT2033-02-15HISTORICAL_CONTEXTComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2033-02-15HISTORICAL_CONTEXTComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2033-12-19HISTORICAL_CONTEXTIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2033-12-19HISTORICAL_CONTEXTIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2035-06-19HISTORICAL_CONTEXTProcess or use limited to a particular indication, combination, regimen, population or formulation; not whole-label anchor.Source
PATENT2035-06-19CANONICAL_ANCHORIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2036-11-08FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2036-11-08FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2036-11-08FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
REGULATORY_STATUS2035-06-19CANONICAL_DECISIONEnglish description not available.Source
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.