Novoeight Purple Book BLA 125466

BLA number
125466
Proprietary names
Novoeight
Proper names
Antihemophilic Factor (Recombinant)
Applicant
Novo Nordisk Inc.
Center
CBER
First observed release
2020-08-01
Latest observed release
2026-06-01
Newest archive release
2026-06-01
FDA patent list
No patents listed in the captured FDA patent list; source updated 2025-06-11
Coverage
Present in newest release

Latest Known Product Presentations#

Product, Proprietary name, Proper name table
ProductProprietary nameProper nameLicense typeStrengthDosage formRoutePresentationMarketingLicensureApprovalPatent list provided
001NovoeightAntihemophilic Factor (Recombinant)351(a)3000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15
002NovoeightAntihemophilic Factor (Recombinant)351(a)2000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15
003NovoeightAntihemophilic Factor (Recombinant)351(a)1500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15
004NovoeightAntihemophilic Factor (Recombinant)351(a)1000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15
005NovoeightAntihemophilic Factor (Recombinant)351(a)250IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15
006NovoeightAntihemophilic Factor (Recombinant)351(a)500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2013-10-15

Published Patent List#

No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.

Official Monthly Change Events#

Release, Event, Product table
ReleaseEventProductNameLicense typeStatusApplicant
2021-05-01U001Novoeight351(a)RxNovo Nordisk Inc.
2021-05-01U002Novoeight351(a)RxNovo Nordisk Inc.
2021-05-01U003Novoeight351(a)RxNovo Nordisk Inc.
2021-05-01U004Novoeight351(a)RxNovo Nordisk Inc.
2021-05-01U005Novoeight351(a)RxNovo Nordisk Inc.
2021-05-01U006Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R001Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R002Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R003Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R004Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R005Novoeight351(a)RxNovo Nordisk Inc.
2020-08-01R006Novoeight351(a)RxNovo Nordisk Inc.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-08-01001Novoeight351(a)RxLicensed2013-10-15
2020-08-01002Novoeight351(a)RxLicensed2013-10-15
2020-08-01003Novoeight351(a)RxLicensed2013-10-15
2020-08-01004Novoeight351(a)RxLicensed2013-10-15
2020-08-01005Novoeight351(a)RxLicensed2013-10-15
2020-08-01006Novoeight351(a)RxLicensed2013-10-15