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Product profile · United States

DOCETAXEL

 ·  Patent Litigation & Settlement History ↓

IngredientDOCETAXEL
Application typeNDA
Application201195
Product005
Dosage formINJECTABLE
RouteINJECTION
Strength160MG/8ML (20MG/ML)
Approval date2012-04-20
Marketing statusPrescription
Status event—
ApplicantACCORD HLTHCARE
Product source

Current GenericRadar decision

Year2017
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2017-08-09
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2017-08-09
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
207252 / 003FINAL_APPROVAL · FINAL_APPROVED2017-08-09—JIANGSU HENGRUI PHARMACEUTICALS CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
209640 / 003FINAL_APPROVAL · FINAL_APPROVED2018-01-19—AMNEAL EU LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208137 / 001FINAL_APPROVAL · FINAL_APPROVED2019-04-01—MYLAN LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210327 / 003FINAL_APPROVAL · FINAL_APPROVED2019-05-16—ADAPTIS PHARMA PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216677 / 003FINAL_APPROVAL · FINAL_APPROVED2024-11-26—HERITAGE PHARMACEUTICALS INC DBA AVET PHARMACEUTICALS 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 5 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
207252 / 003JIANGSU HENGRUI PHARMACEUTICALS CO LTDFINAL_APPROVAL · FINAL_APPROVED2017-08-09 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
209640 / 003AMNEAL EU LTDFINAL_APPROVAL · FINAL_APPROVED2018-01-19 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208137 / 001MYLAN LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2019-04-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210327 / 003ADAPTIS PHARMA PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2019-05-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
216677 / 003HERITAGE PHARMACEUTICALS INC DBA AVET PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2024-11-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2017-08-09TERMINAL_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.