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Product profile · United States

SPRIX

 ·  Patent Litigation & Settlement History ↓

IngredientKETOROLAC TROMETHAMINE
Application typeNDA
Application022382
Product001
Dosage formSPRAY, METERED
RouteNASAL
Strength15.75MG/SPRAY
Approval date2010-05-14
Marketing statusPrescription
Status event—
ApplicantCOSETTE
Product source

Current GenericRadar decision

Year2013
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2013-05-14
Patent anchor—
Exclusivity anchor2013-05-14
Protection date2018-12-25
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS. Canonical anchor 2013-05-14; tails [{"kind":"PATENT","number_or_code":"US6333044","date":"2018-12-25"}]

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US74766892012-10-11DP/U U-1056NNDP_U
Intranasal ketorolac composition and pain-treatment claims. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US63330442018-12-25DP/U U-1057NNDP_U
Liquid nasal ketorolac composition and associated systemic pain treatment. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NDF2010-05-142013-05-14Original new dosage form, new combination or exact new product approval; covers its approved formulation/use scope at this original approval.YY2013-05-14Source

2026-10-12 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: ANNUALS_2011_2026_REVIEWED

2026-10-10 · NO_RECORD_IN_CURRENT_SNAPSHOT · 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 (4)
TypeDateRoleBasisSource
PATENT2012-10-11LISTING_CONTEXTIntranasal ketorolac composition and pain-treatment claims. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2018-12-25FTO_TAILLiquid nasal ketorolac composition and associated systemic pain treatment. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
REGULATORY_EXCLUSIVITY2013-05-14CANONICAL_ANCHOROriginal new dosage form, new combination or exact new product approval; covers its approved formulation/use scope at this original approval.Source
REGULATORY_STATUS2013-05-14DECISION_BASISPOST_ANCHOR_RIGHTS. Canonical anchor 2013-05-14; tails [{"kind":"PATENT","number_or_code":"US6333044","date":"2018-12-25"}]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.