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Product profile · United States

OPSUMIT

 ·  Patent Litigation & Settlement History ↓

IngredientMACITENTAN
Application typeNDA
Application204410
Product001
Dosage formTABLET
RouteORAL
Strength10MG
Approval date2013-10-18
Marketing statusPrescription
Status event—
ApplicantACTELION
Product source

Current GenericRadar decision

Year2021
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2021-04-06
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2021-04-06
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
70947812025-12-05DS/DP ————
———
70947812026-06-05— ————
—2026-06-05—
109460152026-09-11DP/U U-1445———
———
109460152027-03-11— ————
—2027-03-11—
92657622027-05-29DP/U U-1820———
———
92657622027-11-29— ————
—2027-11-29—
83676852028-10-04DP/U U-1445———
———
83676852029-04-04— ————
—2029-04-04—
82688472029-04-18U U-1446———
———
82688472029-10-18— ————
—2029-10-18—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
M-187—2028-02-28————Source
PED—2028-08-28————Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
214112 / 001APPLICATION_TENTATIVE_OBSERVATION · TENTATIVE_PRODUCT_SCOPE_UNVERIFIED——RHODES PHARMSNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211224 / 001FINAL_APPROVAL · FINAL_APPROVED2021-04-06—ZYDUS LIFESCIENCES GLOBAL FZENEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211198 / 001FINAL_APPROVAL · FINAL_APPROVED2023-04-18—AUROBINDO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211195 / 001FINAL_APPROVAL · FINAL_APPROVED2024-01-09—APOTEX INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211107 / 001FINAL_APPROVAL · FINAL_APPROVED2024-08-05—TORRENT PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211128 / 001FINAL_APPROVAL · FINAL_APPROVED2025-08-18—ALEMBIC PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211136 / 001FINAL_APPROVAL · FINAL_APPROVED2025-08-20—MSN LABORATORIES PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211123 / 001FINAL_APPROVAL · FINAL_APPROVED2025-08-26—SUN PHARMACEUTICAL INDUSTRIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211120 / 001FINAL_APPROVAL · FINAL_APPROVED2025-11-05—LAURUS LABS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211026 / 001FINAL_APPROVAL · FINAL_APPROVED2025-12-03—LEPU PHARMACEUTICAL TECHNOLOGY CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211161 / 001FINAL_APPROVAL · FINAL_APPROVED2025-12-03—MYLAN PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211000 / 001FINAL_APPROVAL · FINAL_APPROVED2026-06-08—AMNEAL EU LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211187 / 001FINAL_APPROVAL · FINAL_APPROVED2026-06-08—TEVA PHARMACEUTICALS USA INCNEXACT_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 12 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
211224 / 001ZYDUS LIFESCIENCES GLOBAL FZEFINAL_APPROVAL · FINAL_APPROVED2021-04-06 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211198 / 001AUROBINDO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2023-04-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211195 / 001APOTEX INCFINAL_APPROVAL · FINAL_APPROVED2024-01-09 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211107 / 001TORRENT PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2024-08-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211128 / 001ALEMBIC PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2025-08-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211136 / 001MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2025-08-20 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211123 / 001SUN PHARMACEUTICAL INDUSTRIES LTDFINAL_APPROVAL · FINAL_APPROVED2025-08-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211120 / 001LAURUS LABS LTDFINAL_APPROVAL · FINAL_APPROVED2025-11-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211026 / 001LEPU PHARMACEUTICAL TECHNOLOGY CO LTDFINAL_APPROVAL · FINAL_APPROVED2025-12-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211161 / 001MYLAN PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2025-12-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211000 / 001AMNEAL EU LTDFINAL_APPROVAL · FINAL_APPROVED2026-06-08 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211187 / 001TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2026-06-08 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2021-04-06TERMINAL_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.

No litigation or settlement record currently linked to this product.