Product Details for: Eylea HD

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravitreal
8MG/0.07ML
Single-Dose Vial
351(a)
Eylea HD
Rx
Proper Name
aflibercept
BLA Number
761355
Applicant
Regeneron Pharmaceuticals, Inc.
Original Approval Date
August 18, 2023
Date of First Licensure
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