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Product profile · United States

Xolair

 ·  Patent Litigation & Settlement History ↓

Ingredientomalizumab
Application typeBLA
Application103976
Product001
Dosage formFor Injection
RouteSubcutaneous
Strength150MG
Approval date2003-06-20
Marketing statusRx
Status event—
ApplicantGenentech, Inc.
Product source

Current GenericRadar decision

Year2015
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeEXCLUSIVITY
Anchor date2015-06-20
Patent anchor—
Exclusivity anchor2015-06-20
Protection date—
First Final ANDA—
Status event—

GNR judgment: DEEP_REVIEW. Reference year: 2015. Anchor type: EXCLUSIVITY. Patent anchor: not recorded. Exclusivity anchor: 2015-06-20. Anchor date: 2015-06-20. 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
100349402025-11-04PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
110782942028-07-08PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
119876372028-07-08PURPLE_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.
———
100177322034-03-14PURPLE_BOOK ————
Original PB source record retained in gnr_patent_source_records. No TRUE_DS/DS-equivalent judgment.
———
106767102034-03-14PURPLE_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.
———
120309592043-07-20PURPLE_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
761399 / 001INTERCHANGEABILITY · INTERCHANGEABLE——CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 001BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-03-07—CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 002INTERCHANGEABILITY · INTERCHANGEABLE——CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 002BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-03-07—CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 003BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-01—CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 003INTERCHANGEABILITY · INTERCHANGEABLE——CELLTRION, Inc.NREFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource
761399 / 003FINAL_APPROVAL · BIOSIMILAR_APPROVED2025-12-01—CELLTRION, Inc.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 4 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
761399 / 001CELLTRION, Inc.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-03-07 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761399 / 002CELLTRION, Inc.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-03-07 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761399 / 003CELLTRION, Inc.BIOSIMILAR_APPROVAL · BIOSIMILAR_APPROVED2025-12-01 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
761399 / 003CELLTRION, Inc.FINAL_APPROVAL · BIOSIMILAR_APPROVED2025-12-01 REFERENCE_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
BLA_PATENT_EXCLUSIVITY_REVIEW—BUSINESS_CLASSIFICATION_WITH_CONDITIONSEnglish description not available.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.