Home PurpleBook 761034 Tecentriq Purple Book BLA 761034
BLA number 761034
Proprietary names Tecentriq
Proper names atezolizumab
Applicant Genentech, Inc.
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 Product Proprietary name Proper name License type Strength Dosage form Route Presentation Marketing Licensure Approval Patent list provided 001 Tecentriq atezolizumab 351(a) 1,200MG/20ML (60MG/ML) Injection Intravenous Single-Dose Vial Rx Licensed 2016-05-18 002 Tecentriq atezolizumab 351(a) 840MG/14ML (60MG/ML) Injection Intravenous Single-Dose Vial Rx Licensed 2019-03-08
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 Release Event Product Name License type Status Applicant 2023-03-01 U 001 Tecentriq 351(a) Rx Genentech, Inc. 2023-03-01 U 002 Tecentriq 351(a) Rx Genentech, Inc. 2020-11-01 U 001 Tecentriq 351(a) Rx Genentech, Inc. 2020-11-01 U 002 Tecentriq 351(a) Rx Genentech, Inc. 2020-08-01 U 001 Tecentriq 351(a) Rx Genentech, Inc. 2020-08-01 U 002 Tecentriq 351(a) Rx Genentech, Inc. 2020-05-01 R 001 Tecentriq 351(a) Rx Genentech, Inc. 2020-05-01 R 002 Tecentriq 351(a) Rx Genentech, Inc.
Observed Product State History# Release, Product, Name table Release Product Name License type Marketing Licensure Approval 2020-05-01 001 Tecentriq 351(a) Rx Licensed 2016-05-18 2020-05-01 002 Tecentriq 351(a) Rx Licensed 2019-03-08
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