Esperoct Purple Book BLA 125671

BLA number
125671
Proprietary names
Esperoct
Proper names
Antihemophilic Factor (Recombinant), GlycoPEGylated-exei
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
001EsperoctAntihemophilic Factor (Recombinant), GlycoPEGylated-exei351(a)3000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2019-02-19
002EsperoctAntihemophilic Factor (Recombinant), GlycoPEGylated-exei351(a)1000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2019-02-19
003EsperoctAntihemophilic Factor (Recombinant), GlycoPEGylated-exei351(a)2000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2019-02-19
004EsperoctAntihemophilic Factor (Recombinant), GlycoPEGylated-exei351(a)500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2019-02-19
005EsperoctAntihemophilic Factor (Recombinant), GlycoPEGylated-exei351(a)1500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2019-02-19

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
2021-05-01U001Esperoct351(a)RxNovo Nordisk Inc.
2021-05-01U002Esperoct351(a)RxNovo Nordisk Inc.
2021-05-01U003Esperoct351(a)RxNovo Nordisk Inc.
2021-05-01U004Esperoct351(a)RxNovo Nordisk Inc.
2021-05-01U005Esperoct351(a)RxNovo Nordisk Inc.
2020-08-01R001Esperoct351(a)RxNovo Nordisk Inc.
2020-08-01R002Esperoct351(a)RxNovo Nordisk Inc.
2020-08-01R003Esperoct351(a)RxNovo Nordisk Inc.
2020-08-01R004Esperoct351(a)RxNovo Nordisk Inc.
2020-08-01R005Esperoct351(a)RxNovo Nordisk Inc.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-08-01001Esperoct351(a)RxLicensed2019-02-19
2020-08-01002Esperoct351(a)RxLicensed2019-02-19
2020-08-01003Esperoct351(a)RxLicensed2019-02-19
2020-08-01004Esperoct351(a)RxLicensed2019-02-19
2020-08-01005Esperoct351(a)RxLicensed2019-02-19