Keytruda Purple Book BLA 125514

BLA number
125514
Proprietary names
Keytruda
Proper names
pembrolizumab
Applicant
MSD International Business GmbH
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
001Keytrudapembrolizumab351(a)50MGFor InjectionIntravenousSingle-Dose VialDiscLicensed2014-09-04
002Keytrudapembrolizumab351(a)100MG/4ML (25MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2015-01-15

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
2026-05-01U001Keytruda351(a)DiscMSD International Business GmbH
2026-05-01U002Keytruda351(a)RxMSD International Business GmbH
2024-08-01U001Keytruda351(a)DiscMerck Sharp & Dohme LLC
2024-08-01U002Keytruda351(a)RxMerck Sharp & Dohme LLC
2024-01-01U001Keytruda351(a)DiscMerck Sharp & Dohme LLC
2024-01-01U002Keytruda351(a)RxMerck Sharp & Dohme LLC
2023-03-01U001Keytruda351(a)DiscMerck Sharp & Dohme LLC
2023-03-01U002Keytruda351(a)RxMerck Sharp & Dohme LLC
2023-01-01U001Keytruda351(a)DiscMerck Sharp & Dohme Corp.
2023-01-01U002Keytruda351(a)RxMerck Sharp & Dohme Corp.
2021-07-01U001Keytruda351(a)DiscMerck Sharp & Dohme Corp.
2021-07-01U002Keytruda351(a)RxMerck Sharp & Dohme Corp.
2020-08-01U001Keytruda351(a)DiscMerck Sharp & Dohme Corp.
2020-08-01U002Keytruda351(a)RxMerck Sharp & Dohme Corp.
2020-05-01R001Keytruda351(a)DiscMerck Sharp & Dohme Corp.
2020-05-01R002Keytruda351(a)RxMerck Sharp & Dohme Corp.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-05-01001Keytruda351(a)DiscLicensed2014-09-04
2020-05-01002Keytruda351(a)RxLicensed2015-01-15