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Ahzantive
aflibercept-mrbb
351(k) Biosimilar
Overview
Source: Purple BookProprietary name
Ahzantive
Proper name
aflibercept-mrbb
Licence type
351(k) Biosimilar
BLA number
761378
Applicant
Formycon AG
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| Strength | Dosage form | Route | Presentation | Status | Licensed |
|---|---|---|---|---|---|
| 2MG/0.05ML | Injection | Intravitreal | Single-Dose Vial | Rx | June 28, 2024 |
| 2MG/0.05ML | Injection | Intravitreal | Pre-Filled Syringe | Rx | April 17, 2025 |
Reference product
Source: Purple BookThis product is licensed with reference to Eylea (aflibercept).
Sources for this page
| Purple Book | FDA | Licence type, presentations, reference product, exclusivity |