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Product profile · United States

OTEZLA

 ·  Patent Litigation & Settlement History ↓

IngredientAPREMILAST
Application typeNDA
Application205437
Product003
Dosage formTABLET
RouteORAL
Strength30MG
Approval date2014-03-21
Marketing statusPrescription
Status event—
ApplicantAMGEN INC
Product source

Current GenericRadar decision

Year2021
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2021-02-17
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2021-02-17
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
74276382028-02-16DS/DP ————
———
74276382028-08-16— ————
—2028-08-16—
125760342033-11-30DP/U U-1858———
———
125760342033-11-30DP/U U-4291———
———
125760342033-11-30DP/U U-4290———
———
100925412034-05-29U U-2659———
———
100925412034-05-29U U-2403———
———
98728542034-05-29U U-2232———
———
98728542034-05-29U U-2233———
———
125760342034-05-30— ————
—2034-05-30—
100925412034-11-29— ————
—2034-11-29—
98728542034-11-29— ————
—2034-11-29—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-248—2026-07-19————Source
M-299—2026-07-20————Source
PED—2027-01-19————Source
PED—2027-01-20————Source
NPP—2027-04-25————Source
PED—2027-10-25————Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
211859 / 003APPLICATION_TENTATIVE_OBSERVATION · TENTATIVE_PRODUCT_SCOPE_UNVERIFIED——ZYDUS PHARMSNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211819 / 003FINAL_APPROVAL · FINAL_APPROVED2021-02-17—UNICHEM LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211782 / 003FINAL_APPROVAL · FINAL_APPROVED2021-06-30—AMNEAL EU LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211761 / 003FINAL_APPROVAL · FINAL_APPROVED2021-09-21—ALKEM LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211897 / 003FINAL_APPROVAL · FINAL_APPROVED2022-08-18—TEVA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211774 / 003FINAL_APPROVAL · FINAL_APPROVED2023-04-07—SHILPA MEDICARE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211756 / 003FINAL_APPROVAL · FINAL_APPROVED2023-07-14—DR REDDYS LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211716 / 003FINAL_APPROVAL · FINAL_APPROVED2023-07-19—AUROBINDO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211878 / 003FINAL_APPROVAL · FINAL_APPROVED2023-07-26—ANNORA PHARMA PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211674 / 003FINAL_APPROVAL · FINAL_APPROVED2023-10-16—GLENMARK PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211734 / 003FINAL_APPROVAL · FINAL_APPROVED2024-02-07—MANKIND PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211788 / 003FINAL_APPROVAL · FINAL_APPROVED2024-11-25—MACLEODS PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211887 / 003FINAL_APPROVAL · FINAL_APPROVED2024-12-16—MSN LABORATORIES PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211834 / 003FINAL_APPROVAL · FINAL_APPROVED2025-06-20—TORRENT 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 13 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
211819 / 003UNICHEM LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2021-02-17 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211782 / 003AMNEAL EU LTDFINAL_APPROVAL · FINAL_APPROVED2021-06-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211761 / 003ALKEM LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2021-09-21 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211897 / 003TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2022-08-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211774 / 003SHILPA MEDICARE LTDFINAL_APPROVAL · FINAL_APPROVED2023-04-07 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211756 / 003DR REDDYS LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2023-07-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211716 / 003AUROBINDO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2023-07-19 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211878 / 003ANNORA PHARMA PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2023-07-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211674 / 003GLENMARK PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2023-10-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211734 / 003MANKIND PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-02-07 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211788 / 003MACLEODS PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2024-11-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211887 / 003MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2024-12-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211834 / 003TORRENT PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2025-06-20 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2021-02-17TERMINAL_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.