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Product profile · United States

TAMIFLU

 ·  Patent Litigation & Settlement History ↓

IngredientOSELTAMIVIR PHOSPHATE
Application typeNDA
Application021246
Product002
Dosage formFOR SUSPENSION
RouteORAL
StrengthEQ 6MG BASE/ML
Approval date2011-03-21
Marketing statusPrescription
Status event—
ApplicantROCHE
Product source

Current GenericRadar decision

Year2017
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2017-09-14
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2017-09-14
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
No exclusivity facts are recorded in this product snapshot.

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
209113 / 001FINAL_APPROVAL · FINAL_APPROVED2017-09-14—ZYDUS PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208823 / 001FINAL_APPROVAL · FINAL_APPROVED2017-10-31—ALVOGEN INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208347 / 001FINAL_APPROVAL · FINAL_APPROVED2018-02-20—LUPIN INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210186 / 001FINAL_APPROVAL · FINAL_APPROVED2018-02-27—AMNEAL PHARMACEUTICALS OF NY LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211125 / 001FINAL_APPROVAL · FINAL_APPROVED2019-02-27—TEVA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212784 / 001FINAL_APPROVAL · FINAL_APPROVED2020-05-27—AJANTA PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212858 / 001FINAL_APPROVAL · FINAL_APPROVED2021-08-30—INVAGEN PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213594 / 001FINAL_APPROVAL · FINAL_APPROVED2022-01-05—SUNSHINE LAKE PHARMA CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211894 / 001FINAL_APPROVAL · FINAL_APPROVED2022-01-13—STRIDES PHARMA GLOBAL PTE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
214949 / 001FINAL_APPROVAL · FINAL_APPROVED2022-02-28—LEADING PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
209590 / 001FINAL_APPROVAL · FINAL_APPROVED2022-03-28—HETERO LABS LTD UNIT VNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215313 / 001FINAL_APPROVAL · FINAL_APPROVED2022-05-02—MSN LABORATORIES PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215538 / 001FINAL_APPROVAL · FINAL_APPROVED2023-02-14—EPIC PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218131 / 001FINAL_APPROVAL · FINAL_APPROVED2024-05-10—AUROBINDO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217303 / 001FINAL_APPROVAL · FINAL_APPROVED2024-07-02—PHARMOBEDIENT CONSULTING LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213695 / 001FINAL_APPROVAL · FINAL_APPROVED2025-03-03—JUBILANT GENERICS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218307 / 001FINAL_APPROVAL · FINAL_APPROVED2026-06-25—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 17 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
209113 / 001ZYDUS PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2017-09-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208823 / 001ALVOGEN INCFINAL_APPROVAL · FINAL_APPROVED2017-10-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208347 / 001LUPIN INCFINAL_APPROVAL · FINAL_APPROVED2018-02-20 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210186 / 001AMNEAL PHARMACEUTICALS OF NY LLCFINAL_APPROVAL · FINAL_APPROVED2018-02-27 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211125 / 001TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2019-02-27 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212784 / 001AJANTA PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2020-05-27 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212858 / 001INVAGEN PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2021-08-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213594 / 001SUNSHINE LAKE PHARMA CO LTDFINAL_APPROVAL · FINAL_APPROVED2022-01-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211894 / 001STRIDES PHARMA GLOBAL PTE LTDFINAL_APPROVAL · FINAL_APPROVED2022-01-13 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
214949 / 001LEADING PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2022-02-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
209590 / 001HETERO LABS LTD UNIT VFINAL_APPROVAL · FINAL_APPROVED2022-03-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215313 / 001MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2022-05-02 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215538 / 001EPIC PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2023-02-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218131 / 001AUROBINDO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-05-10 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217303 / 001PHARMOBEDIENT CONSULTING LLCFINAL_APPROVAL · FINAL_APPROVED2024-07-02 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213695 / 001JUBILANT GENERICS LTDFINAL_APPROVAL · FINAL_APPROVED2025-03-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218307 / 001ALEMBIC PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2026-06-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2017-09-14TERMINAL_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.