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Product profile · United States

MEKINIST

 ·  Patent Litigation & Settlement History ↓

IngredientTRAMETINIB DIMETHYL SULFOXIDE
Application typeNDA
Application204114
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 0.5MG
Approval date2013-05-29
Marketing statusPrescription
Status event—
ApplicantNOVARTIS
Product source

Current GenericRadar decision

Year—
SelectionEXISTING_GENERIC
ReviewCOMPLETED
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2024-08-06
Status event—

Final ANDA candidate 219002/001 on 2024-08-06. Source-level RLD/TE screen; earliest Final and exact Product source reference require independent review.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
73784232027-05-29DS/DP ————
———
73784232027-11-29— ————
—2027-11-29—
87037812030-10-15DS/DP/U U-1712———
———
87037812030-10-15DS/DP/U U-2302———
———
87037812030-10-15DS/DP/U U-2020———
———
87037812030-10-15DS/DP/U U-2305———
———
87037812030-10-15DS/DP/U U-2037———
———
89520182030-10-15U U-2020———
———
87037812031-04-15— ————
—2031-04-15—
89520182031-04-15— ————
—2031-04-15—
85803042032-01-28DP ————
———
91557062032-01-28DP ————
———
92719412032-01-28DP ————
———
93990212032-01-28DP ————
———
85803042032-07-28— ————
—2032-07-28—
91557062032-07-28— ————
—2032-07-28—
92719412032-07-28— ————
—2032-07-28—
93990212032-07-28— ————
—2032-07-28—
108698692033-08-30U U-3184———
———
108698692034-02-28— ————
—2034-02-28—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
I-908—2026-03-16————Source
PED—2026-09-16————Source
ODE-428—2030-03-16————Source
PED—2030-09-16————Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
219002 / 001FINAL_APPROVAL · FINAL_APPROVED2024-08-06—HIKMA PHARMACEUTICALS INTERNATIONAL 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 1 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
219002 / 001HIKMA PHARMACEUTICALS INTERNATIONAL LTDFINAL_APPROVAL · FINAL_APPROVED2024-08-06 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.