Nucala Purple Book BLA 125526

BLA number
125526
Proprietary names
Nucala
Proper names
mepolizumab
Applicant
GlaxoSmithKline LLC
Center
CDER
First observed release
2020-05-01
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
001Nucalamepolizumab351(a)100MGFor InjectionSubcutaneousSingle-Dose VialRxLicensed2015-11-04
002Nucalamepolizumab351(a)100MG/MLInjectionSubcutaneousAutoinjectorRxLicensed2019-06-06
003Nucalamepolizumab351(a)100MG/MLInjectionSubcutaneousPre-Filled SyringeRxLicensed2019-06-06
004Nucalamepolizumab351(a)40MG/0.4MLInjectionSubcutaneousPre-Filled SyringeRxLicensed2022-01-22

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
2022-01-01N004Nucala351(a)RxGlaxoSmithKline LLC
2021-03-01U001Nucala351(a)RxGlaxoSmithKline LLC
2021-03-01U002Nucala351(a)RxGlaxoSmithKline LLC
2021-03-01U003Nucala351(a)RxGlaxoSmithKline LLC
2020-08-01U001Nucala351(a)RxGlaxoSmithKline LLC
2020-08-01U002Nucala351(a)RxGlaxoSmithKline LLC
2020-08-01U003Nucala351(a)RxGlaxoSmithKline LLC
2020-05-01R001Nucala351(a)RxGlaxoSmithKline LLC
2020-05-01R002Nucala351(a)RxGlaxoSmithKline LLC
2020-05-01R003Nucala351(a)RxGlaxoSmithKline LLC

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2022-01-01004Nucala351(a)RxLicensed2022-01-22
2020-05-01001Nucala351(a)RxLicensed2015-11-04
2020-05-01002Nucala351(a)RxLicensed2019-06-06
2020-05-01003Nucala351(a)RxLicensed2019-06-06