On this page

Ogivri

trastuzumab-dkst

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Ogivri
Proper name
trastuzumab-dkst
Licence type
351(k) Biosimilar
BLA number
761074
Applicant
Biocon Biologics Inc.
Center
CDER
Presentations
2
First licensure
—
351(k) biosimilar pathway. This product was licensed as highly similar to a reference product, with no clinically meaningful differences in safety, purity or potency. It is licensed as a biosimilar but is not designated interchangeable, so substitution requires the prescriber.

Presentations

Source: Purple Book
Every strength and presentation recorded in the Purple Book for this product.
Strength Dosage form Route Presentation Status Licensed
150MG For Injection Intravenous Single-Dose Vial Rx April 17, 2019
420MG For Injection Intravenous Multi-Dose Vial Rx December 1, 2017

Reference product

Source: Purple Book

This product is licensed with reference to Herceptin (trastuzumab).

Sources for this page

Purple Book FDA Licence type, presentations, reference product, exclusivity