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Tyruko
natalizumab-sztn
351(k) Biosimilar
Overview
Source: Purple BookProprietary 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| Strength | Dosage form | Route | Presentation | Status | Licensed |
|---|---|---|---|---|---|
| 300MG/15ML (20MG/ML) | Injection | Intravenous | Single-Dose Vial | Rx | August 24, 2023 |
Reference product
Source: Purple BookThis product is licensed with reference to Tysabri (natalizumab).
Sources for this page
| Purple Book | FDA | Licence type, presentations, reference product, exclusivity |