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Product profile · United States

APONVIE

 ·  Patent Litigation & Settlement History ↓

IngredientAPREPITANT
Application typeNDA
Application216457
Product001
Dosage formEMULSION
RouteINTRAVENOUS
Strength32MG/4.4ML (7.2MG/ML)
Approval date2022-09-16
Marketing statusPrescription
Status event—
ApplicantHERON THERAPS INC
Product source

Current GenericRadar decision

Year—
SelectionEXISTING_GENERIC
ReviewCOMPLETED
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2026-03-05
Status event—

ANDA 218851/001 Final 2026-03-05; FDA RLD brand or first generic source. Exact RLD product and competing same-day/earlier ANDAs should be checked.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
105002082035-09-18DP ————
———
106248502035-09-18U U-3440———
———
109530182035-09-18U U-3440———
———
111731182035-09-18DP ————
———
117448002035-09-18DP/U U-3690———
———
118780742035-09-18U U-3787———
———
121152542035-09-18DP ————
———
121152552035-09-18DP ————
———
122905202035-09-18DP ————
———
95612292035-09-18DP/U U-3440———
———
98084652035-09-18U U-3440———
———
99747422035-09-18DP ————
———
99747932035-09-18DP ————
———
99747942035-09-18DP/U U-3440———
———

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
218851 / 001FINAL_APPROVAL · FINAL_APPROVED2026-03-05—MYLAN PHARMACEUTICALS 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
218851 / 001MYLAN PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2026-03-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
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
2025-05-06 Mylan SETTLEMENT 2032-06-01 VERIFIED Source
Earlier license date possible under specified conditions