Rybrevant Faspro Purple Book BLA 761484

BLA number
761484
Proprietary names
Rybrevant Faspro
Proper names
amivantamab and hyaluronidase-lpuj
Applicant
Janssen Biotech, Inc.
Center
CDER
First observed release
2026-02-01
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
001Rybrevant Fasproamivantamab and hyaluronidase-lpuj351(a)1,600MG/10ML; 20,000UNITS/10ML (160MG/2,000UNITS/ML)InjectionSubcutaneousSingle-Dose VialRxLicensed2026-02-13
002Rybrevant Fasproamivantamab and hyaluronidase-lpuj351(a)2,240MG/14ML; 28,000UNITS/14ML (160MG/2,000UNITS/ML)InjectionSubcutaneousSingle-Dose VialRxLicensed2026-02-13
003Rybrevant Fasproamivantamab and hyaluronidase-lpuj351(a)2,400MG/15ML; 30,000UNITS (160MG/2,000UNITS/ML)InjectionSubcutaneousSingle-Dose VialRxLicensed2026-02-13
004Rybrevant Fasproamivantamab and hyaluronidase-lpuj351(a)3,520MG/22ML; 44,000UNITS (160MG/2,000UNITS/ML)InjectionSubcutaneousSingle-Dose VialRxLicensed2026-02-13

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
2026-03-01N001Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-03-01N002Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-03-01N003Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-03-01N004Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-02-01N001Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-02-01N002Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-02-01N003Rybrevant Faspro351(a)RxJanssen Biotech, Inc.
2026-02-01N004Rybrevant Faspro351(a)RxJanssen Biotech, Inc.

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2026-02-01001Rybrevant Faspro351(a)RxLicensed2026-02-13
2026-02-01002Rybrevant Faspro351(a)RxLicensed2026-02-13
2026-02-01003Rybrevant Faspro351(a)RxLicensed2026-02-13
2026-02-01004Rybrevant Faspro351(a)RxLicensed2026-02-13