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EPIOXA CROSS-LINKING (RIBOFLAVIN 5-PHOSPHATE OPHTHALMIC)

GLAUKOS

Summary

FDA approved EPIOXA CROSS-LINKING (RIBOFLAVIN 5-PHOSPHATE OPHTHALMIC) by GLAUKOS. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2025-10-17. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

NDA219910-1

Action Date

2025-10-17

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

EPIOXA CROSS-LINKING (generic: RIBOFLAVIN 5-PHOSPHATE OPHTHALMIC), SOLUTION/DROPS, OPHTHALMIC. Application: NDA219910

Company

Context & Analysis

GLAUKOS has 3 FDA actions in our database, including 1 clearance.

Frequently Asked Questions

How often does GLAUKOS have FDA actions?

GLAUKOS has 3 FDA actions in our database, including 0 recalls and 1 device clearance.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA219910-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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