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Data updated: Mar 10, 2026

CLARINEX-D 12 HOUR

DESLORATADINE Histamine H1 Receptor Antagonists
Approved 2006-02-01
1
Indication
--
Phase 3 Trials
20
Years on Market

Details

Status
Prescription
First Approved
2006-02-01
Routes
ORAL
Dosage Forms
TABLET, EXTENDED RELEASE

Companies

Active Ingredient: DESLORATADINE , PSEUDOEPHEDRINE SULFATE

CLARINEX-D 12 HOUR Approval History

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What CLARINEX-D 12 HOUR Treats

2 indications

CLARINEX-D 12 HOUR is approved for 2 conditions since its original approval in 2006. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Seasonal Allergic Rhinitis
  • Nasal Congestion
Source: FDA Label

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Trial Timeline

Full development history with FDA approval milestones

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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.

CLARINEX-D 12 HOUR FDA Label Details

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Indications & Usage

FDA Label (PDF)

CLARINEX-D 12 HOUR is a combination product containing a histamine-1 (H1) receptor antagonist and an alpha adrenergic agonist indicated for: Relief of nasal and non-nasal symptoms of seasonal allergic rhinitis, including nasal congestion, in adults and adolescents 12 years of age and older. 1.1 Seasonal Allergic Rhinitis CLARINEX-D ® 12 HOUR Extended Release Tablets is indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis, including nasal congestion, in adults and adolescents 12 years of age and older. CLARINEX-D 12 HOUR Extended Release Tablets should be a...

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Data Sources

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