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Product profile · United States

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 ·  Patent Litigation & Settlement History ↓

IngredientPITOLISANT HYDROCHLORIDE
Application typeNDA
Application211150
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 4.45MG BASE
Approval date2019-08-14
Marketing statusPrescription
Status event—
ApplicantHARMONY
Product source

Current GenericRadar decision

Year2026
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2026-07-21
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2026-07-21
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
83544302026-02-06U U-1102———
———
83544302026-02-06U U-1101———
———
84869472029-09-26U U-1102———
———
84869472029-09-26U U-1101———
———
82071972030-03-07DS/DP ————
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-255—2026-08-14————Source
NPP—2027-06-21————Source
ODE-331—2027-10-13————Source
ODE-489—2031-06-21————Source
ODE-519—2033-02-13————Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
218495 / 001FINAL_APPROVAL · FINAL_APPROVED2026-07-21—NOVITIUM PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218846 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-14—LUPIN LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218873 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-14—MSN LABORATORIES PRIVATE LTDNEXACT_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 3 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
218495 / 001NOVITIUM PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2026-07-21 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218846 / 001LUPIN LTDFINAL_APPROVAL · FINAL_APPROVED2026-08-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218873 / 001MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2026-08-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2026-07-21TERMINAL_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
2026-01-01 Hikma SETTLEMENT
Brand-level record; strength scope not established
2030-03 VERIFIED Source
March 2030 conditional on pediatric exclusivity; earlier contingencies; event day unspecified
2025-06-01 Lupin SETTLEMENT
Brand-level record; strength scope not established
2030-01 VERIFIED Source
January 2030 according to June 2025 filing; event day unspecified, may have later amendments
2025-03-31 Annora SETTLEMENT
Brand-level record; strength scope not established
2030-07 VERIFIED Source
July 2030 if pediatric exclusivity; earlier contingencies; older filings stated January 2030, preserve latest