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Product profile · United States

JOENJA

 ·  Patent Litigation & Settlement History ↓

IngredientLENIOLISIB PHOSPHATE
Application typeNDA
Application217759
Product003
Dosage formTABLET
RouteORAL
StrengthEQ 50MG BASE
Approval date2026-09-11
Marketing statusPrescription
Status event—
ApplicantPHARMING
Product source

Current GenericRadar decision

Year2033
SelectionCANDIDATE
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2033-09-11
Patent anchor—
Exclusivity anchor2033-09-11
Protection date2033-09-11
First Final ANDA—
Status event—

NO_POST_ANCHOR_TAIL_IDENTIFIED: Pediatric full-scope statutory orphan end 2033-09-11 is later than the 2032 compound and 2028 moiety-NCE ends. No later applicable issued target or regulatory tail was identified.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
86530922032-02-19CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Historical leniolisib compound end precedes the statutory pediatric orphan anchor.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE—2028-03-24————Source
NS—2029-09-11————Source
ODE*—2030-03-24————Source
ODE2026-09-112033-09-11APDS in patients aged at least 4 years and weighing at least 27 kg; new strengths serve ages 4 to under 12 years.YY2033-09-11—Source

2026-10-13 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: ANNUALS_AND_MONTHLY_REVIEWED

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 (3)
TypeDateRoleBasisSource
PATENT2032-02-19HISTORICAL_CONTEXTHistorical leniolisib compound end precedes the statutory pediatric orphan anchor.Source
REGULATORY_EXCLUSIVITY2033-09-11CANONICAL_ANCHORAPDS in patients aged at least 4 years and weighing at least 27 kg; new strengths serve ages 4 to under 12 years.Source
REGULATORY_STATUS2033-09-11CANONICAL_DECISIONNO_POST_ANCHOR_TAIL_IDENTIFIED: Pediatric full-scope statutory orphan end 2033-09-11 is later than the 2032 compound and 2028 moiety-NCE ends. No later applicable issued target or regulatory tail was identified.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.

No litigation or settlement record currently linked to this product.