Market LIVE
Published markets; coverage varies by country
Product profile · United States

VRAYLAR

 ·  Patent Litigation & Settlement History ↓

IngredientCARIPRAZINE HYDROCHLORIDE
Application typeNDA
Application204370
Product003
Dosage formCAPSULE
RouteORAL
StrengthEQ 4.5MG BASE
Approval date2015-09-17
Marketing statusPrescription
Status event—
ApplicantABBVIE
Product source

Current GenericRadar decision

Year—
SelectionEXISTING_GENERIC
ReviewCOMPLETED
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2022-09-09
Status event—

Final ANDA candidate 213984/003 on 2022-09-09. Source-level RLD/TE screen; earliest Final and exact Product source reference require independent review.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
79436212028-12-16DS/DP ————
———
79436212029-06-16— ————
—2029-06-16—
RE491102029-07-16U U-2544———
———
RE491102029-07-16U U-2543———
———
RE491102029-07-16U U-2545———
———
RE493022029-07-16U U-2544———
———
RE493022029-07-16U U-3503———
———
RE493022029-07-16U U-2545———
———
RE493022029-07-16U U-2543———
———
77371422029-09-17DS/DP/U U-2544———
———
77371422029-09-17DS/DP/U U-2543———
———
77371422029-09-17DS/DP/U U-1750———
———
RE491102030-01-16— ————
—2030-01-16—
RE493022030-01-16— ————
—2030-01-16—
77371422030-03-17— ————
—2030-03-17—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
M-14—2028-12-18————Source
NPP—2028-12-18————Source
PED—2029-06-18————Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
213984 / 003FINAL_APPROVAL · FINAL_APPROVED2022-09-09—ZYDUS WORLDWIDE DMCCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213932 / 003FINAL_APPROVAL · FINAL_APPROVED2022-09-30—SUN PHARMACEUTICAL INDUSTRIES 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 2 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
213984 / 003ZYDUS WORLDWIDE DMCCFINAL_APPROVAL · FINAL_APPROVED2022-09-09 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213932 / 003SUN PHARMACEUTICAL INDUSTRIES LTDFINAL_APPROVAL · FINAL_APPROVED2022-09-30 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.

No litigation or settlement record currently linked to this product.