RecallHawk

IYUZEH (LATANOPROST OPHTHALMIC SOLUTION 0.005%)

THEA PHARMA

Summary

FDA approved IYUZEH (LATANOPROST OPHTHALMIC SOLUTION 0.005%) by THEA PHARMA. NDA (New Drug) approval (Labeling) on 2024-09-16. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

NDA216472-2

Action Date

2024-09-16

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

IYUZEH (generic: LATANOPROST OPHTHALMIC SOLUTION 0.005%), SOLUTION/DROPS, OPHTHALMIC. Application: NDA216472

Context & Analysis

THEA PHARMA has 5 FDA actions in our database.

Frequently Asked Questions

How often does THEA PHARMA have FDA actions?

THEA PHARMA 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 "NDA216472-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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