TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

QUZYTTIR

CETIRIZINE HYDROCHLORIDE
Gastroenterology Approved 2019-10-04
1
Indication
--
Phase 3 Trials
6
Years on Market

Details

Status
Prescription
First Approved
2019-10-04
Routes
INTRAVENOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: CETIRIZINE HYDROCHLORIDE

QUZYTTIR Approval History

Loading approval history...

What QUZYTTIR Treats

1 indications

QUZYTTIR is approved for 1 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Urticaria
Source: FDA Label
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

Loading...
Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

QUZYTTIR FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

QUZYTTIR ® is indicated for the treatment of acute urticaria in adults and children 6 months of age and older. QUZYTTIR ® is a histamine-1 (H 1 ) receptor antagonist indicated for the treatment of acute urticaria in adults and children 6 months of age and older Limitations of Use : Not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function Limitations of use: QUZYTTIR ® is not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function.

QUZYTTIR Patents & Exclusivity

Latest Patent: Feb 2030

Patents (5 active)

US8314083 Expires Feb 28, 2030
US8263581 Expires Feb 28, 2030
US9180090 Expires Feb 11, 2030
US8513259 Expires Feb 11, 2030
US9119771 Expires Feb 11, 2030
Source: FDA Orange Book

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.