Sarclisa Purple Book BLA 761113

BLA number
761113
Proprietary names
Sarclisa
Proper names
isatuximab-irfc
Applicant
Sanofi-Aventis U.S. 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
001Sarclisaisatuximab-irfc351(a)100MG/5ML (20MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2020-03-02
002Sarclisaisatuximab-irfc351(a)500MG/25ML (20MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2020-03-02

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
2024-11-01U001Sarclisa351(a)RxSanofi-Aventis U.S. LLC
2024-11-01U002Sarclisa351(a)RxSanofi-Aventis U.S. LLC
2021-05-01U001Sarclisa351(a)RxSanofi-Aventis U.S. LLC
2021-05-01U002Sarclisa351(a)RxSanofi-Aventis U.S. LLC
2020-08-01U001Sarclisa351(a)Rxsanofi-aventis U.S. LLC
2020-08-01U002Sarclisa351(a)Rxsanofi-aventis U.S. LLC
2020-05-01R001Sarclisa351(a)Rxsanofi-aventis U.S. LLC
2020-05-01R002Sarclisa351(a)Rxsanofi-aventis U.S. LLC

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-05-01001Sarclisa351(a)RxLicensed2020-03-02
2020-05-01002Sarclisa351(a)RxLicensed2020-03-02