Product Details for: Nufymco
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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravitreal
10MG/ML (0.5MG/0.05ML)
Single-Dose Vial
351(k) Interchangeable
Nufymco
Rx
002
Injection
Intravitreal
6MG/ML (0.3MG/0.05ML)
Single-Dose Vial
351(k) Interchangeable
Nufymco
Rx
Proper Name
ranibizumab-leyk
ranibizumab-leyk
Reference Product Proper Name
ranibizumab
ranibizumab
Reference Product Properietary Name
Lucentis
Lucentis
BLA Number
761473
761473
Applicant
Zydus Lifesciences Global FZE
Zydus Lifesciences Global FZE
Original Approval Date
December 18, 2025
December 18, 2025
Date of First Licensure