Xembify Purple Book BLA 125683

BLA number
125683
Proprietary names
Xembify
Proper names
immune globulin subcutaneous, human-klhw
Applicant
Grifols Therapeutics LLC
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
001Xembifyimmune globulin subcutaneous, human-klhw351(a)4GM MG/MLInjectionSubcutaneousSingle-Dose VialRxLicensed2019-07-03
002Xembifyimmune globulin subcutaneous, human-klhw351(a)10GM MG/MLInjectionSubcutaneousSingle-Dose VialRxLicensed2019-07-03
003Xembifyimmune globulin subcutaneous, human-klhw351(a)2GM MG/MLInjectionSubcutaneousSingle-Dose VialRxLicensed2019-07-03
004Xembifyimmune globulin subcutaneous, human-klhw351(a)1GM MG/MLInjectionSubcutaneousSingle-Dose VialRxLicensed2019-07-03

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
2022-05-01U001Xembify351(a)RxGrifols Therapeutics LLC
2022-05-01U002Xembify351(a)RxGrifols Therapeutics LLC
2022-05-01U003Xembify351(a)RxGrifols Therapeutics LLC
2022-05-01U004Xembify351(a)RxGrifols Therapeutics LLC
2021-05-01U001Xembify351(a)RxGrifols Therapeutics LLC
2021-05-01U002Xembify351(a)RxGrifols Therapeutics LLC
2021-05-01U003Xembify351(a)RxGrifols Therapeutics LLC
2021-05-01U004Xembify351(a)RxGrifols Therapeutics LLC
2020-08-01R001Xembify351(a)RxGrifols Therapeutics LLC
2020-08-01R002Xembify351(a)RxGrifols Therapeutics LLC
2020-08-01R003Xembify351(a)RxGrifols Therapeutics LLC
2020-08-01R004Xembify351(a)RxGrifols Therapeutics LLC

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2022-05-01001Xembify351(a)RxLicensed2019-07-03
2022-05-01002Xembify351(a)RxLicensed2019-07-03
2022-05-01003Xembify351(a)RxLicensed2019-07-03
2022-05-01004Xembify351(a)RxLicensed2019-07-03
2020-08-01001Xembify351(a)RxLicensed2019-07-03
2020-08-01002Xembify351(a)RxLicensed2019-07-03
2020-08-01003Xembify351(a)RxLicensed2019-07-03
2020-08-01004Xembify351(a)RxLicensed2019-07-03