RecallHawk

ZYRTEC (CETIRIZINE HYDROCHLORIDE)

KENVUE BRANDS

Summary

FDA approved ZYRTEC (CETIRIZINE HYDROCHLORIDE) by KENVUE BRANDS. NDA (New Drug) approval (Labeling) on 2026-03-24. TABLET, CHEWABLE, ORAL.

Details

Source

Drug Approval

External ID

NDA021621-18

Action Date

2026-03-24

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

ZYRTEC (generic: CETIRIZINE HYDROCHLORIDE), TABLET, CHEWABLE, ORAL. Application: NDA021621

Context & Analysis

KENVUE BRANDS has 3 FDA actions in our database.

Frequently Asked Questions

How often does KENVUE BRANDS have FDA actions?

KENVUE BRANDS 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 "NDA021621-18" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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