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Product profile · United States

VIJOICE

 ·  Patent Litigation & Settlement History ↓

IngredientALPELISIB
Application typeNDA
Application215039
Product001
Dosage formTABLET
RouteORAL
Strength50MG
Approval date2022-04-05
Marketing statusPrescription
Status event—
ApplicantNOVARTIS
Product source

Current GenericRadar decision

Year2033
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2033-04-29
Patent anchor2033-04-29
Exclusivity anchor2029-04-05
Protection date2037-02-17
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_REMAIN; canonical=2033-04-29; exact Final ANDA not directly identified; not generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
84762682029-09-10DS/DP —YNTRUE_DS
| B1C0201 issued-claim review2026-10-14: TRUE_DS
———
84762682029-09-10ORANGE_BOOK —YNTRUE_DS
English description not available.
———
82274622033-04-29DS/DP —YNTRUE_DS
| B1C0201 issued-claim review2026-10-14: TRUE_DS
———
82274622033-04-29ORANGE_BOOK —YNTRUE_DS
English description not available.
———
114330592037-02-17U U-4359NNU
| B1C0201 issued-claim review2026-10-14: U
———
114330592037-02-17ORANGE_BOOK U-4359NNU
English description not available.
———
124271412037-02-17U U-4288NNU
| B1C0201 issued-claim review2026-10-14: U
———
124271412037-02-17ORANGE_BOOK U-4288NNU
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE2019-05-242024-05-24English description not available.YY2024-05-24Source
ODE-3962022-04-052029-04-05English description not available.YY2029-04-05—Source
ODE-3962022-04-052029-04-05English description not available.YY2029-04-05Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · 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 (7)
TypeDateRoleBasisSource
PATENT2029-09-10HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2033-04-29CANONICAL_ANCHOREnglish description not available.Source
PATENT2037-02-17FTO_TAILEnglish description not available.Source
PATENT2037-02-17FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_STATUS2033-04-29CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_REMAIN; canonical=2033-04-29; exact Final ANDA not directly identified; not generic absenceSource
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.