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Product profile · United States

AKYNZEO

 ·  Patent Litigation & Settlement History ↓

IngredientFOSNETUPITANT CHLORIDE HYDROCHLORIDE; PALONOSETRON HYDROCHLORIDE
Application typeNDA
Application210493
Product002
Dosage formSOLUTION
RouteINTRAVENOUS
StrengthEQ 235MG BASE/20ML (EQ 11.75MG BASE/ML);EQ 0.25MG BASE/20ML (EQ 0.0125MG BASE/ML)
Approval date2020-05-27
Marketing statusPrescription
Status event—
ApplicantHELSINN HLTHCARE
Product source

Current GenericRadar decision

Year2032
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typePATENT
Anchor date2032-05-23
Patent anchor2032-05-23
Exclusivity anchor2023-04-19
Protection date—
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
91863572030-11-18U U-2301NYDS_EQUIVALENT
———
108282972030-12-17U U-2301NYDS_EQUIVALENT
———
102080732032-05-23U U-2301NYDS_EQUIVALENT
———
107177212032-05-23DS —YNTRUE_DS
———
113126982032-05-23DS/DP —NNDP
———
84264502032-05-23DS/DP —YNTRUE_DS
———
88955862032-05-23U U-2301NYDS_EQUIVALENT
———
94037722032-05-23DS/U U-2301YNTRUE_DS
———
99089072032-05-23DS/DP —YNTRUE_DS
———
106249112037-06-02DP —NNDP
———
115293622037-06-02DP —NNDP
———
122081092037-06-02DP —NNDP
———

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 (1)
TypeDateRoleBasisSource
REGULATORY_STATUS2032-05-23CANONICAL_DECISIONPOST_ANCHOR_RIGHTSSource
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.