Eloctate Purple Book BLA 125487

BLA number
125487
Proprietary names
Eloctate
Proper names
Antihemophilic Factor (Recombinant), Fc Fusion protein
Applicant
Bioverativ Therapeutics, 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
001EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)1500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
002EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)1000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
003EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)2000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
004EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)3000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
005EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)750IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
006EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)500IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
007EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)250IUFor InjectionIntravenousSingle-Dose VialRxLicensed2014-06-06
008EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)5000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2017-01-27
009EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)6000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2017-01-27
010EloctateAntihemophilic Factor (Recombinant), Fc Fusion protein351(a)4000IUFor InjectionIntravenousSingle-Dose VialRxLicensed2017-01-27

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
2021-09-01U001Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U002Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U003Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U004Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U005Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U006Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U007Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U008Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U009Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-09-01U010Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U001Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U002Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U003Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U004Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U005Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U006Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U007Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U008Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U009Eloctate351(a)RxBioverativ Therapeutics, Inc.
2021-05-01U010Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R001Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R002Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R003Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R004Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R005Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R006Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R007Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R008Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R009Eloctate351(a)RxBioverativ Therapeutics, Inc.
2020-08-01R010Eloctate351(a)RxBioverativ Therapeutics, Inc.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-08-01001Eloctate351(a)RxLicensed2014-06-06
2020-08-01002Eloctate351(a)RxLicensed2014-06-06
2020-08-01003Eloctate351(a)RxLicensed2014-06-06
2020-08-01004Eloctate351(a)RxLicensed2014-06-06
2020-08-01005Eloctate351(a)RxLicensed2014-06-06
2020-08-01006Eloctate351(a)RxLicensed2014-06-06
2020-08-01007Eloctate351(a)RxLicensed2014-06-06
2020-08-01008Eloctate351(a)RxLicensed2017-01-27
2020-08-01009Eloctate351(a)RxLicensed2017-01-27
2020-08-01010Eloctate351(a)RxLicensed2017-01-27