Market LIVE
Published markets; coverage varies by country
Product profile · United States

SEIZALAM

 ·  Patent Litigation & Settlement History ↓

IngredientMIDAZOLAM HYDROCHLORIDE
Application typeNDA
Application209566
Product001
Dosage formSOLUTION
RouteINTRAMUSCULAR
StrengthEQ 50MG BASE/10ML (EQ 5MG BASE/ML)
Approval date2018-09-14
Marketing statusDiscontinued
Status event—
ApplicantMMT
Product source

Current GenericRadar decision

Year2025
SelectionDISQUALIFIED
ReviewFINAL
Anchor typeFDA_MARKETING_STATUS
Anchor date—
Patent anchor—
Exclusivity anchor2025-09-14
Protection date2025-09-14
First Final ANDA—
Status event—

FDA_DISCONTINUED; RIGHTS_CANONICAL=2025 CANDIDATE; NO_IDENTIFIED_POST_ANCHOR_TAIL

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
No patent facts are recorded for this product.

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-2072018-09-142025-09-14Status epilepticus in adults, all approved SEIZALAM indication; Selective waiver for Rafa midazolam autoinjector documented 2021-04-16; not blanket exclusivity cancellation.YY2025-09-14—Source

2026-10-12 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: ANNUALS_AND_MONTHLY_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 (2)
TypeDateRoleBasisSource
REGULATORY_EXCLUSIVITY2025-09-14SCOPE_CONTEXTStatus epilepticus in adults, all approved SEIZALAM indication; Selective waiver for Rafa midazolam autoinjector documented 2021-04-16; not blanket exclusivity cancellation.Source
REGULATORY_STATUS—TERMINAL_STATUSFDA_DISCONTINUED; RIGHTS_CANONICAL=2025 CANDIDATE; NO_IDENTIFIED_POST_ANCHOR_TAILSource
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.