RecallHawk

QUZYTTIR (CETIRIZINE HYDROCHLORIDE)

ESTEVE

Summary

FDA approved QUZYTTIR (CETIRIZINE HYDROCHLORIDE) by ESTEVE. NDA (New Drug) approval (Labeling) on 2025-07-28. SOLUTION, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA211415-8

Action Date

2025-07-28

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

QUZYTTIR (generic: CETIRIZINE HYDROCHLORIDE), SOLUTION, INTRAVENOUS. Application: NDA211415

Company

Context & Analysis

ESTEVE has 3 FDA actions in our database.

Frequently Asked Questions

How often does ESTEVE have FDA actions?

ESTEVE has 3 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 "NDA211415-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions