On this page

Tyruko

natalizumab-sztn

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Tyruko
Proper name
natalizumab-sztn
Licence type
351(k) Biosimilar
BLA number
761322
Applicant
Sandoz Inc.
Center
CDER
Presentations
1
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
300MG/15ML (20MG/ML) Injection Intravenous Single-Dose Vial Rx August 24, 2023

Reference product

Source: Purple Book

This product is licensed with reference to Tysabri (natalizumab).

Sources for this page

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