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Product profile · United States

IMVEXXY

 ·  Patent Litigation & Settlement History ↓

IngredientESTRADIOL
Application typeNDA
Application208564
Product001
Dosage formINSERT
RouteVAGINAL
Strength0.004MG
Approval date2018-05-29
Marketing statusPrescription
Status event—
ApplicantMAYNE PHARMA
Product source

Current GenericRadar decision

Year2025
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2025-12-08
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2025-12-08
Status event—

Exact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
102586302032-11-21U U-2317———
———
102586302032-11-21U U-2316———
———
103987082032-11-21U U-2614———
———
103987082032-11-21U U-2317———
———
104710722032-11-21U U-2316———
———
104710722032-11-21U U-2317———
———
105375812032-11-21DP/U U-2316———
———
105375812032-11-21DP/U U-2317———
———
105688912032-11-21U U-2316———
———
105688912032-11-21U U-2317———
———
106680822032-11-21U U-2317———
———
106680822032-11-21U U-2316———
———
108066972032-11-21DP ————
———
108354872032-11-21U U-2316———
———
108354872032-11-21U U-2317———
———
108885162032-11-21U U-2317———
———
108885162032-11-21U U-2316———
———
110651972032-11-21DP ————
———
111167172032-11-21DP ————
———
111232832032-11-21DP ————
———
112414452032-11-21U U-2316———
———
112414452032-11-21U U-2317———
———
112468752032-11-21U U-2316———
———
112468752032-11-21U U-2317———
———
113049592032-11-21DP ————
———
113511822032-11-21U U-2316———
———
113511822032-11-21U U-2317———
———
91800912032-11-21DP/U U-2317———
———
91800912032-11-21DP/U U-2316———
———
92893822032-11-21DP ————
———
112666612034-02-02U U-2316———
———
112666612034-02-02U U-2317———
———

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
214137 / 001FINAL_APPROVAL · FINAL_APPROVED2025-12-08—TEVA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource

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 1 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
214137 / 001TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2025-12-08 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2025-12-08TERMINAL_GENERIC_BASISExact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.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.

Event datePartyEvent Licensed entryEvidenceSource
2026-10-16 Teva Pharmaceuticals USA SETTLEMENT
Brand-level record; strength scope not established
2032-09-02 SOURCE_CONFIRMED Source
tracking_id=US-N208564-TEVA-20261016-SETTLEMENT; 발행사 ASX 공시. 법원 승인 조건 및 특정 조기진입 예외. 최장 특허 2034-02 언급과 별개인 회사별 허용일. 현재 master/판정 미확인.; verified source 2026-10-24. No Final approval, global legal anchor or actual launch inferred.