Reblozyl Purple Book BLA 761136

BLA number
761136
Proprietary names
Reblozyl
Proper names
luspatercept-aamt
Applicant
Celgene Corporation, a Bristol-Myers Squibb Company
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
001Reblozylluspatercept-aamt351(a)25MG/VIALFor InjectionSubcutaneousSingle-Dose VialRxLicensed2019-11-08
002Reblozylluspatercept-aamt351(a)75MG/VIALFor InjectionSubcutaneousSingle-Dose VialRxLicensed2019-11-08

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
2023-11-01U001Reblozyl351(a)RxCelgene Corporation, a Bristol-Myers Squibb Company
2023-11-01U002Reblozyl351(a)RxCelgene Corporation, a Bristol-Myers Squibb Company
2021-11-01U001Reblozyl351(a)RxCelgene Corporation, a Bristol-Myers Squibb Company
2021-11-01U002Reblozyl351(a)RxCelgene Corporation, a Bristol-Myers Squibb Company
2020-08-01U001Reblozyl351(a)RxCelgene Corporation
2020-08-01U002Reblozyl351(a)RxCelgene Corporation
2020-05-01R001Reblozyl351(a)RxCelgene Corporation
2020-05-01R002Reblozyl351(a)RxCelgene Corporation

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-05-01001Reblozyl351(a)RxLicensed2019-11-08
2020-05-01002Reblozyl351(a)RxLicensed2019-11-08