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Product profile · United States

Lucentis

 ·  Patent Litigation & Settlement History ↓

Ingredientranibizumab
Application typeBLA
Application125156
Product002
Dosage formInjection
RouteIntravitreal
Strength6MG/ML (0.3MG/0.05ML)
Approval date2012-08-10
Marketing statusDisc*
Status event—
ApplicantGenentech, Inc.
Product source

Current GenericRadar decision

Year2023
SelectionDISCONTINUED
ReviewFINAL
Anchor typePRODUCT_STATUS
Anchor date2023-08-17
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA—
Status event2023-08-17

GNR judgment: DISCONTINUED. Reference year: 2023. Anchor type: PRODUCT_STATUS. Patent anchor: not recorded. Exclusivity anchor: not recorded. Anchor date: 2023-08-17. Patent tail: not established. Exclusivity tail: not established. Review status: FINAL. Historical detailed rationale is retained in the evidence snapshot; this is a structured English summary, not a literal translation.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
67166022021-11-01PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
68281212022-07-08PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
96887752022-12-31PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
69216592023-10-17PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
83837732023-12-13PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
85748692028-07-08PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
104219842033-09-19PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
97653792034-03-10PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
100177322034-03-14PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
108297322034-03-14PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
101129942035-11-05PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
No exclusivity facts are recorded in this product snapshot.

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
761202 / 001BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2021-09-17—Samsung Bioepis Co., Ltd.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761165 / 001INTERCHANGEABILITY · INTERCHANGEABLE——Sandoz Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761165 / 001BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2022-08-02—Sandoz Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761165 / 002INTERCHANGEABILITY · INTERCHANGEABLE——Sandoz Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761165 / 002BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2022-08-02—Sandoz Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761202 / 001INTERCHANGEABILITY · INTERCHANGEABLE——Samsung Bioepis Co., Ltd.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761473 / 001INTERCHANGEABILITY · INTERCHANGEABLE——Zydus Lifesciences Global FZENREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761473 / 001BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-18—Zydus Lifesciences Global FZENREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761473 / 002BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-18—Zydus Lifesciences Global FZENREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761473 / 002INTERCHANGEABILITY · INTERCHANGEABLE——Zydus Lifesciences Global FZENREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 001BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02—Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 001INTERCHANGEABILITY · INTERCHANGEABLE——Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 002BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02—Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 002INTERCHANGEABILITY · INTERCHANGEABLE——Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 003INTERCHANGEABILITY · INTERCHANGEABLE——Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 003BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02—Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 004BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02—Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761480 / 004INTERCHANGEABILITY · INTERCHANGEABLE——Lupin Limited (Biotech Division)NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761202 / 002BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-09-04—Samsung Bioepis Co., Ltd.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761202 / 002INTERCHANGEABILITY · INTERCHANGEABLE——Samsung Bioepis Co., Ltd.NREFERENCE_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 10 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
761202 / 001Samsung Bioepis Co., Ltd.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2021-09-17 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761165 / 001Sandoz Inc.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2022-08-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761165 / 002Sandoz Inc.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2022-08-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761473 / 001Zydus Lifesciences Global FZEBIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-18 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761473 / 002Zydus Lifesciences Global FZEBIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-18 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761480 / 001Lupin Limited (Biotech Division)BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761480 / 002Lupin Limited (Biotech Division)BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761480 / 003Lupin Limited (Biotech Division)BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761480 / 004Lupin Limited (Biotech Division)BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-06-02 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761202 / 002Samsung Bioepis Co., Ltd.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2026-09-04 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
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.