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Nyvepria

pegfilgrastim-apgf

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Nyvepria
Proper name
pegfilgrastim-apgf
Licence type
351(k) Biosimilar
BLA number
761111
Applicant
Hospira Inc., a Pfizer Company
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
6MG/0.6ML Injection Subcutaneous Pre-Filled Syringe Rx June 10, 2020

Reference product

Source: Purple Book

This product is licensed with reference to Neulasta (pegfilgrastim).

Sources for this page

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