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Product profile · United States

MOTEGRITY

 ·  Patent Litigation & Settlement History ↓

IngredientPRUCALOPRIDE SUCCINATE
Application typeNDA
Application210166
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 1MG BASE
Approval date2018-12-14
Marketing statusPrescription
Status event—
ApplicantTAKEDA PHARMS USA
Product source

Current GenericRadar decision

Year2024
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2024-12-26
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2024-12-26
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
No patent facts are recorded for this product.

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
M-14—2028-07-10————Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
218492 / 001FINAL_APPROVAL · FINAL_APPROVED2024-12-26—NOVITIUM PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217662 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—HIKMA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218177 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—MSN LABORATORIES PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218295 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—ALKEM LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218778 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—TORRENT PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218795 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—ZENARA PHARMA PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218812 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—AMNEAL PHARMACEUTICALS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218847 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—LUPIN LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218963 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—APPCO PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218977 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—APOTEX INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219078 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—SOMERSET THERAPEUTICS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219160 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—ANNORA PHARMA PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219193 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—SPECGX LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219216 / 001FINAL_APPROVAL · FINAL_APPROVED2025-06-24—BIONPHARMA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218056 / 001FINAL_APPROVAL · FINAL_APPROVED2025-08-07—ZYDUS LIFESCIENCES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219220 / 001FINAL_APPROVAL · FINAL_APPROVED2026-01-16—AJANTA PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219071 / 001FINAL_APPROVAL · FINAL_APPROVED2026-02-05—TEVA PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219180 / 001FINAL_APPROVAL · FINAL_APPROVED2026-06-29—MICRO LABS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219234 / 001FINAL_APPROVAL · FINAL_APPROVED2026-07-27—ALEMBIC PHARMACEUTICALS 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 19 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
218492 / 001NOVITIUM PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2024-12-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217662 / 001HIKMA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218177 / 001MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218295 / 001ALKEM LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218778 / 001TORRENT PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218795 / 001ZENARA PHARMA PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218812 / 001AMNEAL PHARMACEUTICALS LLCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218847 / 001LUPIN LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218963 / 001APPCO PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218977 / 001APOTEX INCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219078 / 001SOMERSET THERAPEUTICS LLCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219160 / 001ANNORA PHARMA PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219193 / 001SPECGX LLCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219216 / 001BIONPHARMA INCFINAL_APPROVAL · FINAL_APPROVED2025-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218056 / 001ZYDUS LIFESCIENCES LTDFINAL_APPROVAL · FINAL_APPROVED2025-08-07 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219220 / 001AJANTA PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2026-01-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219071 / 001TEVA PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2026-02-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219180 / 001MICRO LABS LTDFINAL_APPROVAL · FINAL_APPROVED2026-06-29 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219234 / 001ALEMBIC PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2026-07-27 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2024-12-26TERMINAL_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.