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Product profile · United States

ORIAHNN (COPACKAGED)

 ·  Patent Litigation & Settlement History ↓

IngredientELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM
Application typeNDA
Application213388
Product001
Dosage formCAPSULE
RouteORAL
StrengthEQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE
Approval date2020-05-29
Marketing statusPrescription
Status event—
ApplicantABBVIE
Product source

Current GenericRadar decision

Year2029
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typePATENT
Anchor date2029-07-06
Patent anchor2029-07-06
Exclusivity anchor2023-07-23
Protection date—
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_EXIST

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
114593052028-11-07DP/U U-2842NNDP
———
74199832029-07-06DS/DP —YNTRUE_DS
———
108816592034-03-14U U-2842NNU
———
110454702034-03-14U U-2842NNU
———
120832272038-08-20DP/U U-2842NNDP
———
115422392039-07-23DS/DP —NNDP
———
116908452040-08-27U U-3655NNU
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NP—2023-05-29Historical Orange Book exclusivity; scope and start date not independently established————Source
NCE—2023-07-23FDA historical NCE 5-year new chemical entity exclusivity. Active-moiety-wide protection against covered follow-on NDA/ANDA applications; not indication-specific. Statutory exceptions or waivers are not excluded by this categorization.YY——Source

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 (1)
TypeDateRoleBasisSource
REGULATORY_STATUS2029-07-06CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_EXISTSource
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.