CHILDREN'S ZYRTEC HIVES RELIEF
CETIRIZINE HYDROCHLORIDE
Approval overview CHILDREN'S ZYRTEC HIVES RELIEF is listed in Drugs@FDA under application 021621 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient CETIRIZINE HYDROCHLORIDE Form and strength TABLET, CHEWABLE;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor KENVUE BRANDS Submission history Latest submission status date: 2026-03-24 00:00:00.
Structured Monograph
Clinical summary
Approval overview CHILDREN'S ZYRTEC HIVES RELIEF is listed in Drugs@FDA under application 021621 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CETIRIZINE HYDROCHLORIDE Form and strength TABLET, CHEWABLE;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor KENVUE BRANDS Submission history Latest submission status date: 2026-03-24 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.