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Product profile · United States

SOVALDI

 ·  Patent Litigation & Settlement History ↓

IngredientSOFOSBUVIR
Application typeNDA
Application212480
Product002
Dosage formPELLETS
RouteORAL
Strength200MG/PACKET
Approval date2019-08-28
Marketing statusPrescription
Status event—
ApplicantGILEAD SCIENCES INC
Product source

Current GenericRadar decision

Year2029
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2029-09-26
Patent anchor2029-09-26
Exclusivity anchor—
Protection date2031-06-11
First Final ANDA—
Status event—

GNR judgment: DEEP_REVIEW. Reference year: 2029. Anchor type: TRUE_DS_PATENT. Patent anchor: 2029-09-26. Exclusivity anchor: not recorded. Anchor date: 2029-09-26. 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
83342702028-03-21DS/DP/U U-1470———
———
85807652028-03-21DS/DP/U U-1470———
———
90855732028-03-21DS/DP/U U-1470———
———
83342702028-09-21— ————
—2028-09-21—
83342702028-09-21ORANGE_BOOK U-1470YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
—2028-09-21—
85807652028-09-21— ————
—2028-09-21—
85807652028-09-21ORANGE_BOOK U-1470YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
—2028-09-21—
90855732028-09-21— ————
—2028-09-21—
90855732028-09-21ORANGE_BOOK U-1470YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
—2028-09-21—
79645802029-03-26DS/DP/U U-1470———
———
86333092029-03-26DS/DP/U U-1470———
———
88891592029-03-26DP/U U-1470———
———
79645802029-09-26— ————
—2029-09-26—
79645802029-09-26ORANGE_BOOK U-1470YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
—2029-09-26—
86333092029-09-26— ————
—2029-09-26—
86333092029-09-26ORANGE_BOOK U-1470YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
—2029-09-26—
88891592029-09-26— ————
—2029-09-26—
88891592029-09-26ORANGE_BOOK U-1470NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
—2029-09-26—
92843422030-09-13DS/DP/U U-1470———
———
86180762030-12-11DS/DP/U U-1470———
———
92843422031-03-13— ————
—2031-03-13—
92843422031-03-13ORANGE_BOOK U-1470NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
—2031-03-13—
86180762031-06-11— ————
—2031-06-11—
86180762031-06-11ORANGE_BOOK U-1470NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
—2031-06-11—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-258—2026-08-28————Source
ODE-258—2026-08-28FDA 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 (9)
TypeDateRoleBasisSource
PATENT2028-09-21HISTORICAL_CONTEXTIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2028-09-21HISTORICAL_CONTEXTIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2028-09-21HISTORICAL_CONTEXTIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2029-09-26CANONICAL_ANCHORIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2029-09-26CANONICAL_ANCHORIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2029-09-26HISTORICAL_CONTEXTComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2031-03-13FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
PATENT2031-06-11FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
REGULATORY_STATUS2029-09-26CANONICAL_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.