RecallHawk

EYLEA (AFLIBERCEPT)

REGENERON PHARMACEUTICALS

Summary

FDA approved EYLEA (AFLIBERCEPT) by REGENERON PHARMACEUTICALS. BLA (Biologic) approval (Labeling) on 2024-10-10. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

BLA125387-87

Action Date

2024-10-10

Status

Approved

Category

drug

Product Code

BLA (Biologic)

Product Description

EYLEA (generic: AFLIBERCEPT), INJECTABLE, INJECTION. Application: BLA125387

Context & Analysis

REGENERON PHARMACEUTICALS has 5 FDA actions in our database.

Frequently Asked Questions

How often does REGENERON PHARMACEUTICALS have FDA actions?

REGENERON PHARMACEUTICALS has 5 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "BLA125387-87" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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