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Product profile · United States

SPINRAZA

 ·  Patent Litigation & Settlement History ↓

IngredientNUSINERSEN SODIUM
Application typeNDA
Application209531
Product003
Dosage formSOLUTION
RouteINTRATHECAL
StrengthEQ 50MG BASE/5ML (EQ 10MG BASE/ML)
Approval date2026-03-27
Marketing statusPrescription
Status event—
ApplicantBIOGEN
Product source

Current GenericRadar decision

Year2030
SelectionCANDIDATE
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2030-12-23
Patent anchor2030-12-23
Exclusivity anchor2029-03-27
Protection date2030-12-23
First Final ANDA—
Status event—

NO_POST_ANCHOR_RIGHTS; canonical=2030-12-23; exact Final ANDA not directly identified; not generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
78386572027-07-11DS/DP —YNTRUE_DS
| B1C0201 issued-claim review2026-10-14: TRUE_DS
———
78386572027-07-11ORANGE_BOOK —YNTRUE_DS
English description not available.
———
97177502030-06-17U U-2094NNU
| B1C0201 issued-claim review2026-10-14: U
———
97177502030-06-17U U-1942NNU
| B1C0201 issued-claim review2026-10-14: U
———
97177502030-06-17U U-1943NNU
| B1C0201 issued-claim review2026-10-14: U
———
97177502030-06-17U U-2093NNU
| B1C0201 issued-claim review2026-10-14: U
———
97177502030-06-17ORANGE_BOOK U-1942 / U-1943 / U-2093 / U-2094NNU
English description not available.
———
89808532030-11-24U U-1941NNU
| B1C0201 issued-claim review2026-10-14: U
———
89808532030-11-24ORANGE_BOOK U-1941NNU
English description not available.
———
83619772030-12-23DS/DP —YNTRUE_DS
| B1C0201 issued-claim review2026-10-14: TRUE_DS
———
83619772030-12-23ORANGE_BOOK —YNTRUE_DS
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NS2026-03-272029-03-27English description not available.YY2029-03-27—Source
NS2026-03-272029-03-27English description not available.YY2029-03-27Source

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

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 0 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
No final-approval records are linked to this product.
Decision evidence (6)
TypeDateRoleBasisSource
PATENT2027-07-11HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2030-06-17HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2030-11-24HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2030-12-23CANONICAL_ANCHOREnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_STATUS2030-12-23CANONICAL_DECISIONNO_POST_ANCHOR_RIGHTS; canonical=2030-12-23; exact Final ANDA not directly identified; not generic absenceSource
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.