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Product profile · United States

CAYSTON

 ·  Patent Litigation & Settlement History ↓

IngredientAZTREONAM
Application typeNDA
Application050814
Product001
Dosage formFOR SOLUTION
RouteINHALATION
Strength75MG/VIAL
Approval date2010-02-22
Marketing statusPrescription
Status event—
ApplicantGILEAD
Product source

Current GenericRadar decision

Year2017
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2017-02-22
Patent anchor—
Exclusivity anchor2017-02-22
Protection date2021-12-20
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS. Canonical anchor 2017-02-22; tails [{"kind":"PATENT","number_or_code":"US7208141","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US7214364","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US7427633","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US8399496","date":"2021-12-20"}]

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US72081412021-12-20DP/U U-1031NNDP_U
Nebulized aztreonam composition and treatment; method claims restrict organisms including multidrug-resistant Pseudomonas. Do not equate this with every approved Pseudomonas infection. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US72143642021-12-20DP —NNDP
Inhalable aztreonam lysinate dry-powder composition; dependent saline-dilution claims must be distinguished from administration of dry powder. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US74276332021-12-20DP/U U-1031NNDP
Aztreonam lysinate aerosolable saline formulation. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US83994962021-12-20DP/U U-1377NNDP_U
Inhalable aztreonam lysinate composition and inhalation method; not a new active-compound monopoly. 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
ODE2010-02-222017-02-22CF-associated Pseudomonas respiratory indication; all approved CAYSTON indications.YY2017-02-22Source

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 (6)
TypeDateRoleBasisSource
PATENT2021-12-20FTO_TAILInhalable aztreonam lysinate dry-powder composition; dependent saline-dilution claims must be distinguished from administration of dry powder. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2021-12-20FTO_TAILAztreonam lysinate aerosolable saline formulation. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2021-12-20FTO_TAILNebulized aztreonam composition and treatment; method claims restrict organisms including multidrug-resistant Pseudomonas. Do not equate this with every approved Pseudomonas infection. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2021-12-20FTO_TAILInhalable aztreonam lysinate composition and inhalation method; not a new active-compound monopoly. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
REGULATORY_EXCLUSIVITY2017-02-22CANONICAL_ANCHORCF-associated Pseudomonas respiratory indication; all approved CAYSTON indications.Source
REGULATORY_STATUS2017-02-22DECISION_BASISPOST_ANCHOR_RIGHTS. Canonical anchor 2017-02-22; tails [{"kind":"PATENT","number_or_code":"US7208141","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US7214364","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US7427633","date":"2021-12-20"},{"kind":"PATENT","number_or_code":"US8399496","date":"2021-12-20"}]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.