Ogivri Purple Book BLA 761074

BLA number
761074
Proprietary names
Ogivri
Proper names
trastuzumab-dkst
Applicant
Biocon Biologics Inc.
Center
CDER
First observed release
2020-02-01
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
001Ogivritrastuzumab-dkst351(k) Biosimilar420MGFor InjectionIntravenousMulti-Dose VialRxLicensed2017-12-01
002Ogivritrastuzumab-dkst351(k) Biosimilar150MGFor InjectionIntravenousSingle-Dose VialRxLicensed2019-04-17

Reference Biological Product#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
103792Herceptintrastuzumab351(a)Disc*2026-06-01

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
2023-06-01U001Ogivri351(k) BiosimilarRxBiocon Biologics Inc.
2023-06-01U002Ogivri351(k) BiosimilarRxBiocon Biologics Inc.
2020-06-01U001Ogivri351(k) BiosimilarRxMylan Pharmaceuticals Inc.
2020-06-01U002Ogivri351(k) BiosimilarRxMylan Pharmaceuticals Inc.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-05-01001Ogivri351(k) BiosimilarRxLicensed2017-12-01
2020-05-01002Ogivri351(k) BiosimilarRxLicensed2019-04-17
2020-02-01001Ogivri351(k) BiosimilarMarketedLicensed2017-12-01
2020-02-01002Ogivri351(k) BiosimilarMarketedLicensed2019-04-17