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Product profile · United States

PREZCOBIX

 ·  Patent Litigation & Settlement History ↓

IngredientCOBICISTAT; DARUNAVIR ETHANOLATE
Application typeNDA
Application205395
Product002
Dosage formTABLET
RouteORAL
Strength150MG;EQ 675MG BASE
Approval date2025-03-21
Marketing statusPrescription
Status event—
ApplicantJANSSEN PRODS
Product source

Current GenericRadar decision

Year2029
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2029-09-03
Patent anchor2029-09-03
Exclusivity anchor—
Protection date2032-10-06
First Final ANDA—
Status event—

POST_ANCHOR_TAIL; Canonical 2029-09-03; latest tail 2032-10-06

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
77006452026-12-26DS/DP ————
———
77006452027-06-26— ————
—2027-06-26—
77006452027-06-26ORANGE_BOOK —NYDS_EQUIVALENT
English description not available.
—2027-06-26—
81483742029-09-03DS/DP/U U-4162———
———
81483742029-09-03ORANGE_BOOK U-4162YNTRUE_DS
Independent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.
———
100397182032-10-06DP ————
———
100397182032-10-06ORANGE_BOOK —NNDP
Composition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
No exclusivity facts are recorded in this product snapshot.

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 (4)
TypeDateRoleBasisSource
PATENT2027-06-26HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2029-09-03CANONICAL_ANCHORIndependent chemical compound claim; no mandatory polymorph/formulation limitation. Matched to FDA exact-product estate.Source
PATENT2032-10-06FTO_TAILComposition, salt, polymorph, dispersion or formulation claim; no automatic DS-equivalent promotion.Source
REGULATORY_STATUS2029-09-03CANONICAL_DECISIONPOST_ANCHOR_TAIL; Canonical 2029-09-03; latest tail 2032-10-06Source
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.